Xu, Zenghui et al. published their research in Shipin Kexue (Beijing, China) in 2012 | CAS: 5444-75-7

2-Ethylhexyl benzoate (cas: 5444-75-7) belongs to esters. Esters are widespread in nature and are widely used in industry. In nature, fats are in general triesters derived from glycerol and fatty acids. Esters are responsible for the aroma of many fruits. Esters contain a carbonyl center, which gives rise to 120° C–C–O and O–C–O angles. Unlike amides, esters are structurally flexible functional groups because rotation about the C–O–C bonds has a low barrier. Their flexibility and low polarity is manifested in their physical properties; they tend to be less rigid (lower melting point) and more volatile (lower boiling point) than the corresponding amides. Formula: C15H22O2

Effect of high hydrostatic pressure and heat sterilization on volatile components in peach juice was written by Xu, Zenghui;Jia, Jianhui;Lu, Xiaolian;Peng, Yijiao;Tian, Xu;Guo, Hong. And the article was included in Shipin Kexue (Beijing, China) in 2012.Formula: C15H22O2 The following contents are mentioned in the article:

In this paper, the effect of high hydrostatic pressure (HHP) and heat sterilization treatments on volatile components in peach juice was investigated. The major volatile components in untreated peach juice were acetic acid, 1-pentanol, 3-methylmethoxy-2-Pr acetate and benzaldehyde. The esters exhibited an increase after HHP treatment, which were acetyl Bu ester and di-Bu phthalate with the content increase by 516.67% and 40.91%, benzaldehyde and nonanal with the content increase by 219.78% and 130.55%. Meanwhile, HHP treatment revealed the occurrence of new compounds such as 3,4-dimethyl-2-hexanone and di-Et phthalate and an obvious loss of alcs. Heat sterilization led to dramatic change of volatile components in peach juice, which exhibited the content decrease of acetyl Bu ester, and complete loss of 1-methoxy-2-Pr acetate, acetic acid, 3-methyl-pentanol and benzyl methanol. However, the increased 2-decen-1-ol (oil flavor) damaged the flavor of peach juice. All of these results indicated that HHP could retain better flavor of peach juice than heat sterilization. This study involved multiple reactions and reactants, such as 2-Ethylhexyl benzoate (cas: 5444-75-7Formula: C15H22O2).

2-Ethylhexyl benzoate (cas: 5444-75-7) belongs to esters. Esters are widespread in nature and are widely used in industry. In nature, fats are in general triesters derived from glycerol and fatty acids. Esters are responsible for the aroma of many fruits. Esters contain a carbonyl center, which gives rise to 120° C–C–O and O–C–O angles. Unlike amides, esters are structurally flexible functional groups because rotation about the C–O–C bonds has a low barrier. Their flexibility and low polarity is manifested in their physical properties; they tend to be less rigid (lower melting point) and more volatile (lower boiling point) than the corresponding amides. Formula: C15H22O2

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Ferreira, K. C. R. et al. published their research in International Journal of Electrochemical Science in 2016 | CAS: 5444-75-7

2-Ethylhexyl benzoate (cas: 5444-75-7) belongs to esters. Carboxylic acid esters of low molecular weight are colourless, volatile liquids with pleasant odours, slightly soluble in water. Acyl chlorides and acid anhydrides alcoholysis is another way to produce esters. Acyl chlorides and acid anhydrides react with alcohols to produce esters. Anydrous conditions are recommended since both acyl chlorides and acid anhydrides react with water.SDS of cas: 5444-75-7

Corrosion inhibition of carbon steel in HCl solution by aqueous brown onion peel extract was written by Ferreira, K. C. R.;Cordeiro, R. F. B.;Nunes, J. C.;Orofino, H.;Magalhaes, M.;Torres, A. G.;D’Elia, E.. And the article was included in International Journal of Electrochemical Science in 2016.SDS of cas: 5444-75-7 The following contents are mentioned in the article:

The effect of aqueous brown onion peel extract on the corrosion process of carbon steel in 1 mol L-1 HCl was examined The electrochem. results, including the displacement of the corrosion potential and the inhibitory action in both anodic and cathodic polarization curves showed that the examined extract acted as mixed-type inhibitor. The results of the electrochem. impedance measurements showed that the Rct values increased in the presence of inhibitor reaching 94% of inhibition efficiency in the presence of 300 mg L-1 of the extract The inhibition efficiency of C-steel in 1 mol L-1 HCl increased as the temperature increased and the apparent activation energy (Ea) of C-steel dissolution decreased in the presence of the extract, which suggest a strong chemisorptive bond between the components present in the onion extract and the metal surface. The extract anal. showed few volatile compounds with 3(2H)-Furanone, 2-hexyl-5-methyl- as the major volatile compound and a nitrogenous base (5-octadecyl-pyrimidine-2,4,6-trione) which may play an important role in the inhibition process. This study involved multiple reactions and reactants, such as 2-Ethylhexyl benzoate (cas: 5444-75-7SDS of cas: 5444-75-7).

2-Ethylhexyl benzoate (cas: 5444-75-7) belongs to esters. Carboxylic acid esters of low molecular weight are colourless, volatile liquids with pleasant odours, slightly soluble in water. Acyl chlorides and acid anhydrides alcoholysis is another way to produce esters. Acyl chlorides and acid anhydrides react with alcohols to produce esters. Anydrous conditions are recommended since both acyl chlorides and acid anhydrides react with water.SDS of cas: 5444-75-7

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Lan, Yi-Bin et al. published their research in Food Chemistry in 2016 | CAS: 5444-75-7

2-Ethylhexyl benzoate (cas: 5444-75-7) belongs to esters. Volatile esters with characteristic odours are used in synthetic flavours, perfumes, and cosmetics. Certain volatile esters are used as solvents for lacquers, paints, and varnishes. Esters contain a carbonyl center, which gives rise to 120° C–C–O and O–C–O angles. Unlike amides, esters are structurally flexible functional groups because rotation about the C–O–C bonds has a low barrier. Their flexibility and low polarity is manifested in their physical properties; they tend to be less rigid (lower melting point) and more volatile (lower boiling point) than the corresponding amides. SDS of cas: 5444-75-7

Striking changes in volatile profiles at sub-zero temperatures during over-ripening of ‘Beibinghong’ grapes in Northeastern China was written by Lan, Yi-Bin;Qian, Xu;Yang, Zhong-Jun;Xiang, Xiao-Feng;Yang, Wei-Xi;Liu, Tao;Zhu, Bao-Qing;Pan, Qiu-Hong;Duan, Chang-Qing. And the article was included in Food Chemistry in 2016.SDS of cas: 5444-75-7 The following contents are mentioned in the article:

The evolution of free and glycosidically bound volatile compounds in ‘Beibinghong’ (Vitis vinifera × Vitis amurensis) grape berries throughout on-vine over-ripening and freezing processes was studied in two vintages. The aroma profiles of ‘Beibinghong’ icewine berries were characterized by C6 compounds, higher alcs. and terpenoids in free fractions and carbonyl compounds, higher alcs., C6 alcs. and terpenoids in bound fractions. With regard to free volatile compounds, there was a decrease in the concentration of C6 compounds, terpenols and norisoprenoids and an increase of terpene oxides during over-ripening process. A striking alteration of volatile profile occurred at sub-zero temperatures, particularly for the free fractions such as C6 alcs., higher alcs. and oxidative terpene derivatives These changes were attributed to a series of reactions (biotransformation, oxidation and anaerobic metabolism) induced by water loss and especially freeze-thaw cycles. PCA revealed temperature and rainfall affected the accumulation of volatile compounds during over-ripening processes. This study involved multiple reactions and reactants, such as 2-Ethylhexyl benzoate (cas: 5444-75-7SDS of cas: 5444-75-7).

2-Ethylhexyl benzoate (cas: 5444-75-7) belongs to esters. Volatile esters with characteristic odours are used in synthetic flavours, perfumes, and cosmetics. Certain volatile esters are used as solvents for lacquers, paints, and varnishes. Esters contain a carbonyl center, which gives rise to 120° C–C–O and O–C–O angles. Unlike amides, esters are structurally flexible functional groups because rotation about the C–O–C bonds has a low barrier. Their flexibility and low polarity is manifested in their physical properties; they tend to be less rigid (lower melting point) and more volatile (lower boiling point) than the corresponding amides. SDS of cas: 5444-75-7

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Strepka, Arron M. et al. published their research in Proceedings of the International Waterborne, High-Solids, and Powder Coatings Symposium in 2007 | CAS: 5444-75-7

2-Ethylhexyl benzoate (cas: 5444-75-7) belongs to esters. Esters perform as high-grade solvents for a broad array of plastics, plasticizers, resins, and lacquers, and are one of the largest classes of synthetic lubricants on the commercial market. Polyesters are important plastics, with monomers linked by ester moieties. Many esters have the potential for conformational isomerism, but they tend to adopt an s-cis (or Z) conformation rather than the s-trans (or E) alternative, due to a combination of hyperconjugation and dipole minimization effects. The preference for the Z conformation is influenced by the nature of the substituents and solvent, if present. Lactones with small rings are restricted to the s-trans (i.e. E) conformation due to their cyclic structure.Application of 5444-75-7

Film-forming aid selection to optimize performance and minimize volatile organic content was written by Strepka, Arron M.;Arendt, William D.;Joshi, Makarand. And the article was included in Proceedings of the International Waterborne, High-Solids, and Powder Coatings Symposium in 2007.Application of 5444-75-7 The following contents are mentioned in the article:

Solvents and highly volatile coalescing aids have traditionally been utilized in waterborne coatings applications to assist in the formation of a continuous film. These materials behave like temporary plasticizers. They soften the polymer long enough to allow coalescence and later evaporate from the coating, leaving behind a durable film. While these materials are effective as film formers, they also contribute significantly to the volatile organic content (VOC) of the coating formulation. More permanent film formation aids are significantly less volatile and can be utilized to promote coalescence. The purpose of this paper is to demonstrate the benefits of incorporating less volatile film-forming aids to lower total formulary VOC. Traditional and new film-formation aid technologies have been evaluated in architectural and industrial waterborne coating formulations to demonstrate advantages. Volatility, low temperature coalescence, freeze thaw stability, blocking resistance, hardness, application and other coating properties are utilized to demonstrate the advantages of this strategy. This study involved multiple reactions and reactants, such as 2-Ethylhexyl benzoate (cas: 5444-75-7Application of 5444-75-7).

2-Ethylhexyl benzoate (cas: 5444-75-7) belongs to esters. Esters perform as high-grade solvents for a broad array of plastics, plasticizers, resins, and lacquers, and are one of the largest classes of synthetic lubricants on the commercial market. Polyesters are important plastics, with monomers linked by ester moieties. Many esters have the potential for conformational isomerism, but they tend to adopt an s-cis (or Z) conformation rather than the s-trans (or E) alternative, due to a combination of hyperconjugation and dipole minimization effects. The preference for the Z conformation is influenced by the nature of the substituents and solvent, if present. Lactones with small rings are restricted to the s-trans (i.e. E) conformation due to their cyclic structure.Application of 5444-75-7

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Krause, Przemyslaw et al. published their research in European Journal of Lipid Science and Technology in 2009 | CAS: 5444-75-7

2-Ethylhexyl benzoate (cas: 5444-75-7) belongs to esters. Esters are widespread in nature and are widely used in industry. In nature, fats are in general triesters derived from glycerol and fatty acids. Esters are responsible for the aroma of many fruits. Esters contain a carbonyl center, which gives rise to 120° C–C–O and O–C–O angles. Unlike amides, esters are structurally flexible functional groups because rotation about the C–O–C bonds has a low barrier. Their flexibility and low polarity is manifested in their physical properties; they tend to be less rigid (lower melting point) and more volatile (lower boiling point) than the corresponding amides. Recommanded Product: 5444-75-7

Chemically and enzymatically catalyzed synthesis of C6-C10 alkyl benzoates was written by Krause, Przemyslaw;Hilterhaus, Lutz;Fieg, Georg;Liese, Andreas;Bornscheuer, Uwe. And the article was included in European Journal of Lipid Science and Technology in 2009.Recommanded Product: 5444-75-7 The following contents are mentioned in the article:

The esterification of benzoic acid with n-hexanol, n-octanol, 2-ethylhexanol and n-decanol was investigated in detail. An anal. of the reaction kinetics of esterification in the presence of different com. available chem. catalysts was carried out. The effects of catalyst type and loading on the reaction rate were studied. Although the considered reaction is bimol., it showed a first-order behavior, and a linear dependence with respect to the catalyst concentration was observed Hence, a new approach is presented to describe the reaction kinetics accurately over a wide range. The application of biotechnol. synthesis applying different enzymes as catalysts offers an interesting alternative besides chem. synthesis. Especially an esterase from Bacillus subtilis immobilized on Sepabeads EC-EP showed high stability and was applied for 2 days in the synthesis of hexyl benzoate. Nevertheless, the chem. reaction route remains superior with respect to the catalyst activities under the applied conditions, which were 25 kU/g for the chem. reaction and 0.7 kU/g for the best enzymic conversion. This study involved multiple reactions and reactants, such as 2-Ethylhexyl benzoate (cas: 5444-75-7Recommanded Product: 5444-75-7).

2-Ethylhexyl benzoate (cas: 5444-75-7) belongs to esters. Esters are widespread in nature and are widely used in industry. In nature, fats are in general triesters derived from glycerol and fatty acids. Esters are responsible for the aroma of many fruits. Esters contain a carbonyl center, which gives rise to 120° C–C–O and O–C–O angles. Unlike amides, esters are structurally flexible functional groups because rotation about the C–O–C bonds has a low barrier. Their flexibility and low polarity is manifested in their physical properties; they tend to be less rigid (lower melting point) and more volatile (lower boiling point) than the corresponding amides. Recommanded Product: 5444-75-7

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Shahzadi, Tayyaba et al. published their research in Journal of the Chemical Society of Pakistan in 2012 | CAS: 5444-75-7

2-Ethylhexyl benzoate (cas: 5444-75-7) belongs to esters. Esters typically have a pleasant smell; those of low molecular weight are commonly used as fragrances and are found in essential oils and pheromones. Liquid esters of low volatility serve as softening agents for resins and plastics. Esters also include many industrially important polymers. Polymethyl methacrylate is a glass substitute sold under the names Lucite and Plexiglas; polyethylene terephthalate is used as a film (Mylar) and as textile fibres sold as Terylene, Fortrel, and Dacron.Category: esters-buliding-blocks

Characterization of chemical isolates of Caryopteris odorata was written by Shahzadi, Tayyaba;Abbasi, Muhammad Athar;Aziz-Ur-Rehman;Riaz, Tauheeda;Khan, Khalid Mohammed;Ahmad, Viqar Uddin;Ashraf, Muhammad;Hussain, Bushra;Ajaib, Muhammad. And the article was included in Journal of the Chemical Society of Pakistan in 2012.Category: esters-buliding-blocks The following contents are mentioned in the article:

The phytochem. investigation of the chloroform soluble fraction of Caryopteris odorata (Ham. ex Roxb.) led to the isolation of one new constituent namely; n-pentadecyl[3-(4-hydroxyphenyl)] propanoate (I). The compounds 2-ethyl-n-hexyl benzoate (2), 2-ethyl-n-hexyl trans-cinnamate (3) bis-dodecylbenzene-1,4-dicarboxylate (4) were reported synthetically but these have been isolated for the first time from a natural source. Similarly, the known constituent like trans-cinnamic acid (5) and cis-cinnamic acid (6), heneicosanoic acid (7), Me tricontanoate (8) and octacosanyl tricontanoate (9) were also obtained for the first time from this plant source. The structures of these compounds were determined by IR, HR-MS, 1H-NMR, 13C-NMR spectroscopy and by comparison with the published data of the closely related compounds These isolates were screened for their antioxidant, anti-urease and anti-tyrosinase activities and results revealed that n-Pentadecyl [3-(4-hydroxyphenyl)] propanoate (1) exhibits good antioxidant potential with low to zero enzyme inhibition activities. This study involved multiple reactions and reactants, such as 2-Ethylhexyl benzoate (cas: 5444-75-7Category: esters-buliding-blocks).

2-Ethylhexyl benzoate (cas: 5444-75-7) belongs to esters. Esters typically have a pleasant smell; those of low molecular weight are commonly used as fragrances and are found in essential oils and pheromones. Liquid esters of low volatility serve as softening agents for resins and plastics. Esters also include many industrially important polymers. Polymethyl methacrylate is a glass substitute sold under the names Lucite and Plexiglas; polyethylene terephthalate is used as a film (Mylar) and as textile fibres sold as Terylene, Fortrel, and Dacron.Category: esters-buliding-blocks

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Jiang, Yi-ming et al. published their research in Shipin Gongye Keji in 2014 | CAS: 5444-75-7

2-Ethylhexyl benzoate (cas: 5444-75-7) belongs to esters. Volatile esters with characteristic odours are used in synthetic flavours, perfumes, and cosmetics. Certain volatile esters are used as solvents for lacquers, paints, and varnishes. Esterification is the general name for a chemical reaction in which two reactants (typically an alcohol and an acid) form an ester as the reaction product. Esters are common in organic chemistry and biological materials.Electric Literature of C15H22O2

Analysis of fermentation rule and aromatic composition of olive wine fermented with different species of yeast strains was written by Jiang, Yi-ming;Li, Ji-tao;Wu, Xue-ying;Shu, Jun-xia;Cheng, Li-ping;Jiang, He-ti. And the article was included in Shipin Gongye Keji in 2014.Electric Literature of C15H22O2 The following contents are mentioned in the article:

Using olive as raw materials, the variations of alc. degree, reducing sugar and total acidity were tracked during the whole fermentation of olive wines fermented with three different species of yeast strains. The aromatic compositions of olive wines were extracted The results showed that alc. degree increased gradually, reducing sugar decreased gradually and total acidity increased then decreased during the whole fermentation process fermented with three different species of yeast strains. The fermentation cycle of alc. active dry yeast was shortest. In the olive wine fermented with Saccharomyces cerevisia 1383, alc. degree was highest, reducing sugar was least and total acidity was least. And 50, 49 and 52 kinds of aromatic compounds were identified in olive wines fermented with the Saccharomyces cerevisia 1383, alc. active dry yeast and Saccharomyces cerevisia 1596, resp., and 35 kinds of aromatic compounds were same in the there olive wines. The main aromatic compositions were isopentanol. It was initially identified that olive wine fermented with the Saccharomyces cerevisia 1383 was best. This study involved multiple reactions and reactants, such as 2-Ethylhexyl benzoate (cas: 5444-75-7Electric Literature of C15H22O2).

2-Ethylhexyl benzoate (cas: 5444-75-7) belongs to esters. Volatile esters with characteristic odours are used in synthetic flavours, perfumes, and cosmetics. Certain volatile esters are used as solvents for lacquers, paints, and varnishes. Esterification is the general name for a chemical reaction in which two reactants (typically an alcohol and an acid) form an ester as the reaction product. Esters are common in organic chemistry and biological materials.Electric Literature of C15H22O2

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Savinova, O. S. et al. published their research in Applied Biochemistry and Microbiology in 2022 | CAS: 5444-75-7

2-Ethylhexyl benzoate (cas: 5444-75-7) belongs to esters. Esters are widespread in nature and are widely used in industry. In nature, fats are in general triesters derived from glycerol and fatty acids. Esters are responsible for the aroma of many fruits. Because of their lack of hydrogen-bond-donating ability, esters do not self-associate. Consequently, esters are more volatile than carboxylic acids of similar molecular weight.Reference of 5444-75-7

Biodestruction of Phthalic Acid Esters by White Rot Fungi was written by Savinova, O. S.;Shabaev, A. V.;Glazunova, O. A.;Eremin, S. A.;Fedorova, T. V.. And the article was included in Applied Biochemistry and Microbiology in 2022.Reference of 5444-75-7 The following contents are mentioned in the article:

The ability of white rot fungi from different ecophysiol. groups (primary wood-destroying saprotroph Trametes hirsuta, secondary wood-destroying saprotroph Steccherinum ochraceum, litter saprotroph Crucibulum laeve, and humic saprotroph Agrocybe praecox) to degrade phthalic acid esters (PAEs) was studied. It was shown that diethylhexyl phthalate (DEHP) with longer and branched hydrocarbon chains was more rapidly biodegraded by wood-destroying saprotrophs such as T. hirsuta and S. ochraceum, with an efficiency of more than 99%. Di-Bu phthalate (DBP), which is less hydrophobic with shorter hydrocarbon units, was most efficiently transformed by the litter saprotroph C. laeve (up to 96.5%). Di-Et phthalate (DEP) proved to be the most toxic to all fungi. T. hirsuta showed the greatest resistance to elevated DEP concentrations in the medium. It has been shown that fungi destroy PAEs with the formation of various metabolites, depending on the composition of the multienzyme complex of the fungus. Among the secondary metabolites, ionol, an antioxidant formed by fungi when PAEs is added to the medium, was found. This study involved multiple reactions and reactants, such as 2-Ethylhexyl benzoate (cas: 5444-75-7Reference of 5444-75-7).

2-Ethylhexyl benzoate (cas: 5444-75-7) belongs to esters. Esters are widespread in nature and are widely used in industry. In nature, fats are in general triesters derived from glycerol and fatty acids. Esters are responsible for the aroma of many fruits. Because of their lack of hydrogen-bond-donating ability, esters do not self-associate. Consequently, esters are more volatile than carboxylic acids of similar molecular weight.Reference of 5444-75-7

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Huang, Ya-wei et al. published their research in Shipin Gongye (Shanghai, China) in 2016 | CAS: 5444-75-7

2-Ethylhexyl benzoate (cas: 5444-75-7) belongs to esters. Esters are widespread in nature and are widely used in industry. In nature, fats are in general triesters derived from glycerol and fatty acids. Esters are responsible for the aroma of many fruits. Many esters have the potential for conformational isomerism, but they tend to adopt an s-cis (or Z) conformation rather than the s-trans (or E) alternative, due to a combination of hyperconjugation and dipole minimization effects. The preference for the Z conformation is influenced by the nature of the substituents and solvent, if present. Lactones with small rings are restricted to the s-trans (i.e. E) conformation due to their cyclic structure.Formula: C15H22O2

Analysis on HS-SPME/GC-MS technology in volatile components of Wuchang rice was written by Huang, Ya-wei;Xu, Jin;Wang, Ruo-lan;Dou, Kang-ning. And the article was included in Shipin Gongye (Shanghai, China) in 2016.Formula: C15H22O2 The following contents are mentioned in the article:

To study the flavor of japonica rice, sticky rice and aromatic rice in the 6 harvest rice of Wuchang zone, the anal. of the volatile components was used by solid-phase microextraction (SPME) and gas chromatog. coupled with mass spectrometry (GC-MS), comparing the difference between the different varieties. The results were drown out as follow: in the anal. of 6 cultivars, the aromatic rice Daohuaxiang 2 was observed to have the highest number of volatile compounds Tongnian 1 had the highest volatile compounds of the sticky rice. Chaochan 16 had the highest volatile compounds of the japonica rice. Except alkanes, cyclohexanol, 3,5-dimethyl-, undecanal, acrylic acid-2-Et ester, tetracosanol compounds and nonanal were only found in aromatic rice in cultivars. While Wuchang japonica rice contained the majority of straight-chain alkanes, only a few of the aldehyde acid esters of volatile compounds were detected. 2-Heptan-4-ol, n-caproic acid vinyl ester, trans-3-nonen-2-one and oxacycloheptadec-8-en-2-one (8z) were not found in other rice except for sticky rice, and these could be considered Wuchang sticky rice flavor compounds This study involved multiple reactions and reactants, such as 2-Ethylhexyl benzoate (cas: 5444-75-7Formula: C15H22O2).

2-Ethylhexyl benzoate (cas: 5444-75-7) belongs to esters. Esters are widespread in nature and are widely used in industry. In nature, fats are in general triesters derived from glycerol and fatty acids. Esters are responsible for the aroma of many fruits. Many esters have the potential for conformational isomerism, but they tend to adopt an s-cis (or Z) conformation rather than the s-trans (or E) alternative, due to a combination of hyperconjugation and dipole minimization effects. The preference for the Z conformation is influenced by the nature of the substituents and solvent, if present. Lactones with small rings are restricted to the s-trans (i.e. E) conformation due to their cyclic structure.Formula: C15H22O2

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Feng, Jun-qi et al. published their research in Guangpu Shiyanshi in 2013 | CAS: 5444-75-7

2-Ethylhexyl benzoate (cas: 5444-75-7) belongs to esters. Esters typically have a pleasant smell; those of low molecular weight are commonly used as fragrances and are found in essential oils and pheromones. Many esters have the potential for conformational isomerism, but they tend to adopt an s-cis (or Z) conformation rather than the s-trans (or E) alternative, due to a combination of hyperconjugation and dipole minimization effects. The preference for the Z conformation is influenced by the nature of the substituents and solvent, if present. Lactones with small rings are restricted to the s-trans (i.e. E) conformation due to their cyclic structure.Reference of 5444-75-7

Analysis of flavoring compositions for DuKang wine by GC-MS was written by Feng, Jun-qi;Zhang, Yong-sheng;Wei, Xin-jun. And the article was included in Guangpu Shiyanshi in 2013.Reference of 5444-75-7 The following contents are mentioned in the article:

The flavor compositions that were extracted from DuKang wine by liquid-liquid extraction method were analyzed by gas chromatog.-mass spectrometry (GC-MS). Thirty-nine kinds of flavoring compositions were identified, including 22 kinds of esters, 8 kinds of acids, 6 kinds of alcs. and 2 kinds of alkanes. The main components were Et caproate, Et lactate, caproic acid, acetic acid and Et butyrate. This study involved multiple reactions and reactants, such as 2-Ethylhexyl benzoate (cas: 5444-75-7Reference of 5444-75-7).

2-Ethylhexyl benzoate (cas: 5444-75-7) belongs to esters. Esters typically have a pleasant smell; those of low molecular weight are commonly used as fragrances and are found in essential oils and pheromones. Many esters have the potential for conformational isomerism, but they tend to adopt an s-cis (or Z) conformation rather than the s-trans (or E) alternative, due to a combination of hyperconjugation and dipole minimization effects. The preference for the Z conformation is influenced by the nature of the substituents and solvent, if present. Lactones with small rings are restricted to the s-trans (i.e. E) conformation due to their cyclic structure.Reference of 5444-75-7

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics