McCoull, William et al. published their research in Bioorganic & Medicinal Chemistry Letters in 2012 | CAS: 206559-36-6

3-Benzyloxyphenylisothiocyanate (cas: 206559-36-6) 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. 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.Synthetic Route of C14H11NOS

Identification, optimisation and in vivo evaluation of oxadiazole DGAT-1 inhibitors for the treatment of obesity and diabetes was written by McCoull, William;Addie, Matthew S.;Birch, Alan M.;Birtles, Susan;Buckett, Linda K.;Butlin, Roger J.;Bowker, Suzanne S.;Boyd, Scott;Chapman, Stephen;Davies, Robert D. M.;Donald, Craig S.;Green, Clive P.;Jenner, Chloe;Kemmitt, Paul D.;Leach, Andrew G.;Moody, Graeme C.;Morentin Gutierrez, Pablo;Newcombe, Nicholas J.;Nowak, Thorsten;Packer, Martin J.;Plowright, Alleyn T.;Revill, John;Schofield, Paul;Sheldon, Chris;Stokes, Steve;Turnbull, Andrew V.;Wang, Steven J. Y.;Whalley, David P.;Matthew Wood, J.. And the article was included in Bioorganic & Medicinal Chemistry Letters in 2012.Synthetic Route of C14H11NOS This article mentions the following:

A novel series of DGAT-1 inhibitors was discovered from an oxadiazole amide high throughput screening (HTS) hit. Optimization of potency and ligand lipophilicity efficiency (LLE) resulted in a carboxylic acid containing clin. candidate 53 (AZD3988, I), which demonstrated excellent DGAT-1 potency (0.6 nM), good pharmacokinetics and pre-clin. in vivo efficacy that could be rationalised through a PK/PD relationship. In the experiment, the researchers used many compounds, for example, 3-Benzyloxyphenylisothiocyanate (cas: 206559-36-6Synthetic Route of C14H11NOS).

3-Benzyloxyphenylisothiocyanate (cas: 206559-36-6) 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. 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.Synthetic Route of C14H11NOS

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

Tsuji, Hiroaki et al. published their research in Tetrahedron Letters in 2021 | CAS: 10203-58-4

Diethyl isobutylmalonate (cas: 10203-58-4) belongs to esters. Esters are also usually derived from carboxylic acids. It may also be obtained by reaction of acid anhydride or acid halides with alcohols or by the reaction of salts of carboxylic acids with alkyl halides. 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. Electric Literature of C11H20O4

Nickel-catalyzed hydroalkylation of 1,3-dienes with malonates using a homoallyl carbonate as the 1,3-diene and hydride source was written by Tsuji, Hiroaki;Takahashi, Yoshiyuki;Kawatsura, Motoi. And the article was included in Tetrahedron Letters in 2021.Electric Literature of C11H20O4 This article mentions the following:

The nickel-catalyzed hydroalkylation of 1,3-dienes with malonates using homoallyl carbonates RCH(OCOOCH3)CH2CH=CH2 (R = 4-chlorophenyl, piperonyl, cyclohexyl, etc.) as the 1,3-diene and hydride source was reported. A broad range of homoally carbonates and malonate derivatives R1CH(COOR2)2 (R1 = H, Ph, Me, i-Bu, etc.; R2 = Et, i-Pr, Me, Bn, t-Bu) was well tolerated under a Ni/DPEphos catalyst system, providing the corresponding 1,2-hydroalkylation products RCH=CH2CH(CH3)CH((COOCH3)2)CH3 in 40-94% yields with excellent regioselectivity. Also, suggested the possible reaction mechanism for the nickel-catalyzed hydroalkylation of in situ generated 1,3-dienes with malonates is suggested. In the experiment, the researchers used many compounds, for example, Diethyl isobutylmalonate (cas: 10203-58-4Electric Literature of C11H20O4).

Diethyl isobutylmalonate (cas: 10203-58-4) belongs to esters. Esters are also usually derived from carboxylic acids. It may also be obtained by reaction of acid anhydride or acid halides with alcohols or by the reaction of salts of carboxylic acids with alkyl halides. 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. Electric Literature of C11H20O4

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

Abe, Kyuji et al. published their research in Tanabe Seiyaku Kenkyu Nenpo in 1957 | CAS: 10203-58-4

Diethyl isobutylmalonate (cas: 10203-58-4) 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.Related Products of 10203-58-4

Intravenous anesthetics of thiobarbital series. VI. Synthesis of sodium 5-allyl-5-isobutyl-2-thiobarbiturate was written by Abe, Kyuji;Matsui, Kazuo. And the article was included in Tanabe Seiyaku Kenkyu Nenpo in 1957.Related Products of 10203-58-4 This article mentions the following:

Na (11.5 g.) in 200 cc. EtOH is warmed with 80 g. CH2(CO2Et)2 at 40-50°, and the mixture treated with 102 g. iso-BuI over 4 hrs. to afford 74.5 g. di-Et isobutylmalonate (I), b7 95-8°. I (45 g.), 4.8 g. Na, and 150 cc. EtOH is warmed to 40-50°, 24.8 g. allyl bromide added over 1 hr., and the mixture boiled 3 hrs. to afford 45.6 g. di-Et isobutylallylmalonate (II), b7 114-16°. Isobutylation of di-Et allylmalonate also affords II in 81.9% yield. NCCH2CO2Et (57 g.) in a mixture of 11.5 g. Na and 300 cc. alc. treated with 102 g. iso-BuI affords 46.7 g. Et isobutylcyanoacetate (III), b9 93-7°. α-Chloroisocaproic acid (15 g.) in 50 cc. H2O is neutralized by NaHCO3, heated with 13 g. KCN, evaporated to dryness, a mixture of 26 cc. alc. and 20 cc. concentrated H2SO4 added, and the solution boiled 4 hrs. and distilled in vacuo to afford 7.5 g. III. III (42 g.), 5.7 g. Na, and 200 cc. EtOH is treated with 31 g. allyl bromide to afford 41.6 g. Et isobutylallylcyanoacetate (IV), b10 114-16°. IV (41.6 g.) and 30 g. thiourea in a mixture of 9.2 g. Na and 150 cc. EtOH boiled 6 hrs. and worked up gave 5-isobutyl-5-allyl-4-imino-2-thiobarbiturate (V), yellow, m. 276-8° (dioxane). V is boiled with 150 g. 30% H2SO4 to yield 24 g. 5-isobutyl-5-allyl-2-thiobarbiturate (VI), leaves, m. 145-7° (benzene). II (185 g.) and 110 g. thiourea boiled 7 hrs. with a mixture of 33.2 g. Na and 700 cc. MeOH yield VI. VI Na salt, a light yellow powder, is very hygroscopic and soluble in H2O, and useful as an ultra-short-acting intravenous anesthetic. In the experiment, the researchers used many compounds, for example, Diethyl isobutylmalonate (cas: 10203-58-4Related Products of 10203-58-4).

Diethyl isobutylmalonate (cas: 10203-58-4) 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.Related Products of 10203-58-4

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

Krishna Reddy, Singarajanahalli Mundarinti et al. published their research in Tetrahedron Letters in 2021 | CAS: 33166-79-9

Ethyl 3-oxo-3-(m-tolyl)propanoate (cas: 33166-79-9) belongs to esters. Esters are also usually derived from carboxylic acids. It may also be obtained by reaction of acid anhydride or acid halides with alcohols or by the reaction of salts of carboxylic acids with alkyl halides. 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. Reference of 33166-79-9

Palladium catalyzed hydrolysis-free arylation of aliphatic nitriles for the synthesis of 4-arylquinolin-2-one/pyrazolone derivatives was written by Krishna Reddy, Singarajanahalli Mundarinti;Prasanna Kumari, Subramaniyan;Selva Ganesan, Subramaniapillai. And the article was included in Tetrahedron Letters in 2021.Reference of 33166-79-9 This article mentions the following:

Palladium catalyzed addition of arylboronic acid to the readily available 2-cyano-(N-aryl)-acetamide or ethyl-2-cyanoacetate followed by subsequent reaction transform them into the biol. significant 4-arylquinolin-2-one or pyrazolone derivatives The reaction conditions are robust enough to prevent the hydrolysis of ester/amide moiety during arylation. In addition, the unactivated nitrile moiety in the acetonitrile also converted to the corresponding acetophenone derivative In the experiment, the researchers used many compounds, for example, Ethyl 3-oxo-3-(m-tolyl)propanoate (cas: 33166-79-9Reference of 33166-79-9).

Ethyl 3-oxo-3-(m-tolyl)propanoate (cas: 33166-79-9) belongs to esters. Esters are also usually derived from carboxylic acids. It may also be obtained by reaction of acid anhydride or acid halides with alcohols or by the reaction of salts of carboxylic acids with alkyl halides. 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. Reference of 33166-79-9

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

Choudhari, S. R. et al. published their research in Journal of the Indian Chemical Society in 1978 | CAS: 33166-79-9

Ethyl 3-oxo-3-(m-tolyl)propanoate (cas: 33166-79-9) 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. Cyclic esters are called lactones, regardless of whether they are derived from an organic or inorganic acid. One example of an organic lactone is γ-valerolactone.SDS of cas: 33166-79-9

Synthesis of 2-aminothiazole derivatives was written by Choudhari, S. R.;Goswami, D. D.;Thakar, K. A.. And the article was included in Journal of the Indian Chemical Society in 1978.SDS of cas: 33166-79-9 This article mentions the following:

Fourteen I [R = 4,2-Cl(HO)C6H3 3,4-Cl2C6H3, 2,5-BrMeC6H3, etc.; R1 = H] were prepared by cyclocondensation of acetophenones, 2-haloacetophenones, and benzoylacetate esters with thiourea. Six I (R1 = p-H2NC6H4SO2) were prepared from the resp. I (R1 = H). The hypo- and hyperglycemic activity of nine I were tabulated. In the experiment, the researchers used many compounds, for example, Ethyl 3-oxo-3-(m-tolyl)propanoate (cas: 33166-79-9SDS of cas: 33166-79-9).

Ethyl 3-oxo-3-(m-tolyl)propanoate (cas: 33166-79-9) 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. Cyclic esters are called lactones, regardless of whether they are derived from an organic or inorganic acid. One example of an organic lactone is γ-valerolactone.SDS of cas: 33166-79-9

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

Song, Chengling et al. published their research in Dalton Transactions in 2016 | CAS: 313648-56-5

Dimethyl 5-ethynylisophthalate (cas: 313648-56-5) 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. 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.Category: esters-buliding-blocks

High methane storage and working capacities in a NbO-type metal-organic framework was written by Song, Chengling;Liu, Huimin;Jiao, Jingjing;Bai, Dongjie;Zhou, Wei;Yildirim, Taner;He, Yabing. And the article was included in Dalton Transactions in 2016.Category: esters-buliding-blocks This article mentions the following:

To improve methane adsorption by pore structure optimization, we developed a new organic linker and used it to construct a NbO-type metal-organic framework ZJNU-53 that, after activation, exhibits exceptionally high methane storage and working capacities of 241 and 190 cm3 (STP) cm-3 at 298 K and 65 bar, resp., if the packing loss is not considered, which are among the highest reported for MOF materials. In the experiment, the researchers used many compounds, for example, Dimethyl 5-ethynylisophthalate (cas: 313648-56-5Category: esters-buliding-blocks).

Dimethyl 5-ethynylisophthalate (cas: 313648-56-5) 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. 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.Category: esters-buliding-blocks

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

Jia, Wei et al. published their research in Food Research International in 2022 | CAS: 106-79-6

Dimethyl decanedioate (cas: 106-79-6) belongs to esters. Carboxylic acid esters of low molecular weight are colourless, volatile liquids with pleasant odours, slightly soluble in water. 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.SDS of cas: 106-79-6

Molecular mechanism of high pressure shear grinding on Feng-flavour Chinese Baijiu ageing was written by Jia, Wei;Fan, Zibian;Du, An;Shi, Lin. And the article was included in Food Research International in 2022.SDS of cas: 106-79-6 This article mentions the following:

Ultrahigh-pressure homogenization is a powerful technique for accelerating Baijiu ageing. In this study, the mol. mechanism of artificial ageing was thoroughly investigated utilizing foodomics combined with a mass spectrum information optimization program. Various characterizations of compounds in the ageing process were performed through ultra high performance liquid chromatog. quadrupole-orbitrap high resolution mass spectrometry (UHPLC-Q-Orbitrap) based colloid theoretics. High-pressure shear grinding provides a high-pressure and high-temperature environment for Baijiu, accelerating the formation of flavor compounds and the decomposition of odor and harmful substances, thus improving the sensory characteristics of Feng-flavor Baijiu and shortening the ageing time. A total of 2069 substances were identified according to fragment spectra and Bayesian network model-based peak distribution. Mols. with VIP > 1, including 14 esters, 10 acids, 4 ketones, 3 aldehydes, 2 alcs. and 2 phenols, were quantified as potential markers of chemometric anal. A novel prediction model for Baijiu ageing degree was furnished, and ageing years of Feng-flavor Chinese Baijiu were accurately predicted by factor anal. with KMO 0.784 and a polynomial regression model with r 0.94. The results demonstrated that in 400 bar, fresh distilled Baijiu could reach a natural ageing effect of 6.43 years, which was consistent with the sensory evaluation. In the experiment, the researchers used many compounds, for example, Dimethyl decanedioate (cas: 106-79-6SDS of cas: 106-79-6).

Dimethyl decanedioate (cas: 106-79-6) belongs to esters. Carboxylic acid esters of low molecular weight are colourless, volatile liquids with pleasant odours, slightly soluble in water. 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.SDS of cas: 106-79-6

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

Khusnutdinov, R. I. et al. published their research in Russian Journal of Organic Chemistry in 2017 | CAS: 106-79-6

Dimethyl decanedioate (cas: 106-79-6) belongs to esters. Esters are also usually derived from carboxylic acids. It may also be obtained by reaction of acid anhydride or acid halides with alcohols or by the reaction of salts of carboxylic acids with alkyl halides. Cyclic esters are called lactones, regardless of whether they are derived from an organic or inorganic acid. One example of an organic lactone is γ-valerolactone.Recommanded Product: 106-79-6

Methylation of mono- and dicarboxylic acids with dimethyl carbonate catalyzed with binder-free zeolite NaY was written by Khusnutdinov, R. I.;Shchadneva, N. A.;Mayakova, Yu. Yu.;Konovalova, Yu. S.;Khazipova, A. N.;Kutepov, B. I.. And the article was included in Russian Journal of Organic Chemistry in 2017.Recommanded Product: 106-79-6 This article mentions the following:

Me mono- and dicarboxylates were synthesized by treating the corresponding acids with di-Me carbonate in the presence of a heterogenic catalyst, crystalline aluminosilicate whose mech. strong granules were built of 90-95% of crystal aggregates of zeolite Y with modulus of about 5.0 in the Na-form. Optimum catalyst and reagent ratio and the reaction conditions were found for the preparation of Me esters of mono- and dicarboxylic acids in high yields. In the experiment, the researchers used many compounds, for example, Dimethyl decanedioate (cas: 106-79-6Recommanded Product: 106-79-6).

Dimethyl decanedioate (cas: 106-79-6) belongs to esters. Esters are also usually derived from carboxylic acids. It may also be obtained by reaction of acid anhydride or acid halides with alcohols or by the reaction of salts of carboxylic acids with alkyl halides. Cyclic esters are called lactones, regardless of whether they are derived from an organic or inorganic acid. One example of an organic lactone is γ-valerolactone.Recommanded Product: 106-79-6

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

Walpole, Christopher S. J. et al. published their research in Journal of Medicinal Chemistry in 1993 | CAS: 3903-40-0

12-Methoxy-12-oxododecanoic acid (cas: 3903-40-0) 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. 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.Safety of 12-Methoxy-12-oxododecanoic acid

Analogs of capsaicin with agonist activity as novel analgesic agents; structure-activity studies. 3. The hydrophobic side-chain “C-region” was written by Walpole, Christopher S. J.;Wrigglesworth, Roger;Bevan, Stuart;Campbell, Elizabeth A.;Dray, Andy;James, Iain F.;Masdin, Kay J.;Perkins, Martin N.;Winter, Janet. And the article was included in Journal of Medicinal Chemistry in 1993.Safety of 12-Methoxy-12-oxododecanoic acid This article mentions the following:

Structural variants of the hydrophobic side chain (C region) of the capsaicin mol. have been incorporated into a series of vanillylamides and vanillylthioureas. These compounds have been tested in an in vitro assay for agonism (45Ca2+ influx into dorsal root ganglia neurons), previously shown to be predictive of analgesic activity. The results of this study have established the requirement for a hydrophobic substituent of limited size (molar refractivity, MR, <55) in order to obtain high potency. Combination of the information about the C-region of the capsaicin mol. with studies of the other parts of the mol. provides a rational basis for the design of compounds of increased potency. In the experiment, the researchers used many compounds, for example, 12-Methoxy-12-oxododecanoic acid (cas: 3903-40-0Safety of 12-Methoxy-12-oxododecanoic acid).

12-Methoxy-12-oxododecanoic acid (cas: 3903-40-0) 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. 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.Safety of 12-Methoxy-12-oxododecanoic acid

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

Cabanas-Garcia, Emmanuel et al. published their research in Molecules in 2019 | CAS: 106-79-6

Dimethyl decanedioate (cas: 106-79-6) 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. 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: 106-79-6

Phytochemical profiling of Coryphantha macromeris (cactaceae) growing in greenhouse conditions using ultra-high-performance liquid chromatography-tandem mass spectrometry was written by Cabanas-Garcia, Emmanuel;Areche, Carlos;Jauregui-Rincon, Juan;Cruz-Sosa, Francisco;Balch, Eugenio Perez-Molphe. And the article was included in Molecules in 2019.SDS of cas: 106-79-6 This article mentions the following:

Chromatog. separationcombined with mass spectrometry is a powerful tool for the characterization of plant metabolites because of its high sensitivity and selectivity. In this work, the phytochem.profile of aerial and radicular parts of Coryphantha macromeris (Engelm.) Britton & Rose growing under greenhouse conditions was qual.investigated for the first time by means of modern ultra-high-performance liquid chromatog. tandem mass spectrometry (UHPLC-PDA-HESI-Orbitrap-MS/MS). The UHPLC-PDA-HESI-Orbitrap-MS/MS anal. indicated a high complexity in phenolic metabolites. In our investigation, 69 compounds were detected and 60 of them were identified. Among detected compounds, several phenolic acids, phenolic glycosides, and organic acids were found. Within this diversity, 26 metabolites were exclusively detected in the aerial part, and 19 in the roots. Twenty-four metabolites occurred in both plant parts. According to the relative abundance of peaks in the chromatogram, ferulic and piscidic acids and their derivatives may correspond to one of the main phenolic compounds of C.macromeris. Our results contribute to the phytochem.knowledge regarding C.macromeris and its potential applications in the pharmaceutical and cosmetic industries. Besides, some metabolites and their fragmentation patterns are reported here for the first time for cacti species. In the experiment, the researchers used many compounds, for example, Dimethyl decanedioate (cas: 106-79-6SDS of cas: 106-79-6).

Dimethyl decanedioate (cas: 106-79-6) 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. 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: 106-79-6

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