Category: 763-69-9

Development of a combinatorial/high-throughput workflow for the study of porous polymer networks was written by Majumdar, Partha;Bahr, James A.;Lee, Elizabeth;Kallam, Alekhya;Gubbins, Nathan;Chisholm, Bret J.. And the article was included in PMSE Preprints in 2009.Quality Control of Ethyl 3-ethoxypropanoate The following contents are mentioned in the article:

A high-throughput approach was used to prepare a series of porous epoxy resins. Micro-scale porosity was obtained using high levels of porogens (decane, decanol) with limited miscibility with the polymer. This study involved multiple reactions and reactants, such as Ethyl 3-ethoxypropanoate (cas: 763-69-9Quality Control of Ethyl 3-ethoxypropanoate).

Ethyl 3-ethoxypropanoate (cas: 763-69-9) 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. 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.Quality Control of Ethyl 3-ethoxypropanoate

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

Lithium bromide-catalyzed solvent-free method for synthesis of 2-substituted benzimidazoles and imidazopyridines was written by Dekhane, Deepak V.;Pawar, Shivaji S.;Gupta, Sunil V.;Shingare, Murlidhar S.;Thore, Shivaji N.. And the article was included in Chinese Chemical Letters in 2010.Related Products of 763-69-9 The following contents are mentioned in the article:

The first successful lithium bromide mediated solvent-free condensation of arylenediamine and esters to obtain 2-substituted benzimidazole and imidazopyridine in good to excellent yields was described. This study involved multiple reactions and reactants, such as Ethyl 3-ethoxypropanoate (cas: 763-69-9Related Products of 763-69-9).

Ethyl 3-ethoxypropanoate (cas: 763-69-9) 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. 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 763-69-9

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

Correction to “Predicting Flash Points of Pure Compounds and Mixtures with COSMO-RS” [Erratum to document cited in CA164:106271] was written by Reinisch, Jens;Klamt, Andreas. And the article was included in Industrial & Engineering Chemistry Research in 2016.SDS of cas: 763-69-9 The following contents are mentioned in the article:

The final conversion within eq 4 in the original manuscript is incorrect; The correct equation has been given. There is an analog error in eq 11; The corrected equation has been given. This study involved multiple reactions and reactants, such as Ethyl 3-ethoxypropanoate (cas: 763-69-9SDS of cas: 763-69-9).

Ethyl 3-ethoxypropanoate (cas: 763-69-9) 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.SDS of cas: 763-69-9

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

Oxa-Michael addition promoted by the aqueous sodium carbonate was written by Guo, Shi-Huan;Xing, Sheng-Zhu;Mao, Shuai;Gao, Ya-Ru;Chen, Wen-Liang;Wang, Yong-Qiang. And the article was included in Tetrahedron Letters in 2014.Recommanded Product: 763-69-9 The following contents are mentioned in the article:

An efficient Michael addition of alcs. to activated alkenes promoted by sodium carbonate with water as reaction medium has been developed. The reaction provides a general, economical and environmentally friendly approach for the synthesis of β-alkoxycarbonyl compounds This study involved multiple reactions and reactants, such as Ethyl 3-ethoxypropanoate (cas: 763-69-9Recommanded Product: 763-69-9).

Ethyl 3-ethoxypropanoate (cas: 763-69-9) 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 are more polar than ethers but less polar than alcohols. They participate in hydrogen bonds as hydrogen-bond acceptors, but cannot act as hydrogen-bond donors, unlike their parent alcohols. This ability to participate in hydrogen bonding confers some water-solubility.Recommanded Product: 763-69-9

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

Development of high performance waterborne two component polyurethane topcoat was written by Zhang, Yi. And the article was included in Shanghai Tuliao in 2014.Formula: C7H14O3 The following contents are mentioned in the article:

The raw materials selection and development process of waterborne two component polyurethane topcoat were introduced. The influences of hydroxyl containing dispersions, curing agent, additive and cosolvent etc. on the gloss and fullness of film were discussed. This study involved multiple reactions and reactants, such as Ethyl 3-ethoxypropanoate (cas: 763-69-9Formula: C7H14O3).

Ethyl 3-ethoxypropanoate (cas: 763-69-9) 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 are more polar than ethers but less polar than alcohols. They participate in hydrogen bonds as hydrogen-bond acceptors, but cannot act as hydrogen-bond donors, unlike their parent alcohols. This ability to participate in hydrogen bonding confers some water-solubility.Formula: C7H14O3

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

A simple and efficient copper oxide-catalyzed Barbier-Grignard reaction of unactivated aryl or alkyl bromides with ester was written by Gao, Fei;Deng, Xiang-Jun;Tang, Yu;Tang, Jin-Peng;Yang, Jun;Zhang, Yuan-Ming. And the article was included in Tetrahedron Letters in 2014.COA of Formula: C7H14O3 The following contents are mentioned in the article:

Tertiary alc. compounds were synthesized by Barbier-Grignard reaction of unactivated alkyl or aryl bromides with esters in THF at 65° catalyzed by CuO in good to high yields. The reaction is highly chemoselective. The mechanism involving the leaving group of R²O^–group is discussed. This study involved multiple reactions and reactants, such as Ethyl 3-ethoxypropanoate (cas: 763-69-9COA of Formula: C7H14O3).

Ethyl 3-ethoxypropanoate (cas: 763-69-9) 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. 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.COA of Formula: C7H14O3

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

Novel amine-catalyzed hydroalkoxylation reactions of activated alkenes and alkynes was written by Murtagh, Julie E.;McCooey, Seamus H.;Connon, Stephen J.. And the article was included in Chemical Communications (Cambridge, United Kingdom) in 2005.Quality Control of Ethyl 3-ethoxypropanoate The following contents are mentioned in the article:

Substoichiometric loadings of DBU, catalyzed the efficient 1,4-addition of alcs. and non-nucleophilic amines such as pyrrole to activated alkenes. The application of this methodol. in a one-pot synthesis of a natural product I, and as a strategy for the synthesis of mono-protected 1,3-carbonyl compounds is reported. This study involved multiple reactions and reactants, such as Ethyl 3-ethoxypropanoate (cas: 763-69-9Quality Control of Ethyl 3-ethoxypropanoate).

Ethyl 3-ethoxypropanoate (cas: 763-69-9) 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. 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.Quality Control of Ethyl 3-ethoxypropanoate

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

N Alkylation of Tosylamides Using Esters as Primary and Tertiary Alkyl Sources: Mediated by Hydrosilanes Activated by a Ruthenium Catalyst was written by Nishikata, Takashi;Nagashima, Hideo. And the article was included in Angewandte Chemie, International Edition in 2012.Synthetic Route of C7H14O3 The following contents are mentioned in the article:

In this synthetic methods article, we have developed unique C-N bond-forming reactions by using esters as an alkyl source in the presence of hydrosilanes and a ruthenium catalyst. This reaction is applicable to cyclization reactions producing azacarbocycles. Addnl. applications and studies into the mechanism are currently underway. This study involved multiple reactions and reactants, such as Ethyl 3-ethoxypropanoate (cas: 763-69-9Synthetic Route of C7H14O3).

Ethyl 3-ethoxypropanoate (cas: 763-69-9) 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.Synthetic Route of C7H14O3

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

Use of chromato-mass-spectrometry in combination with solid-phase extraction for analysis of products of cognac manufacturing was written by Markovskiy, M. G.. And the article was included in Izvestiya Vysshikh Uchebnykh Zavedenii, Pishchevaya Tekhnologiya in 2013.Application In Synthesis of Ethyl 3-ethoxypropanoate The following contents are mentioned in the article:

The technique of anal. of cognac products composition on the basis of chromato-mass-spectrometry in combination with solid-phase extraction, able to identify a wide range of components production is investigated. Math. modeling, including a selection of important components and construction of the equations of linear regression to determine the age of products is carried out. This study involved multiple reactions and reactants, such as Ethyl 3-ethoxypropanoate (cas: 763-69-9Application In Synthesis of Ethyl 3-ethoxypropanoate).

Ethyl 3-ethoxypropanoate (cas: 763-69-9) 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. Application In Synthesis of Ethyl 3-ethoxypropanoate

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

Characterization of volatile and semi-volatile compounds in Chinese rice wines by headspace solid phase microextraction followed by gas chromatography-mass spectrometry was written by Luo, Tao;Fan, Wenlai;Xu, Yan. And the article was included in Journal of the Institute of Brewing in 2008.Related Products of 763-69-9 The following contents are mentioned in the article:

The volatile and semi-volatile compounds of Chinese rice wines were extracted by headspace solid phase microextraction (HS-SPME) and analyzed by gas chromatog.-mass spectrum (GC-MS). The original Chinese rice wine samples were diluted with deionized water to a final concentration of 6% (volume/volume) ethanol and then extracted by HS-SPME. The samples were pre-equilibrated at 50°C for 15 min and extracted with stirring at the same temperature for 45 min prior to injection into a GC-MS. A total of 97 volatile and semi-volatile compounds were identified from ten Chinese typical rice wine samples, including 13 alcs., 8 acids, 28 esters, 4 aldehydes and ketones, 17 aromatic compounds, 3 lactones, 6 phenols, 3 sulfides, 9 furans and 6 nitrogen-containing compounds, of which, 39 compounds were firstly reported in Chinese rice wine. By stepwise linear discrimination anal., the ten Chinese rice wine samples could be classified into three groups according to the production area, and in particular, the production technologies. This study involved multiple reactions and reactants, such as Ethyl 3-ethoxypropanoate (cas: 763-69-9Related Products of 763-69-9).

Ethyl 3-ethoxypropanoate (cas: 763-69-9) 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. Related Products of 763-69-9

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