Bohnert, T. et al. published their research in Journal of Vinyl & Additive Technology in 2000 | 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. 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.Application In Synthesis of 2-Ethylhexyl benzoate

Unique benzoate plasticizer for reducing viscosity and fusion temperature was written by Bohnert, T.;Stanhope, B.;Gruszecki, K.;Pitman, S.;Elsworth, V.. And the article was included in Journal of Vinyl & Additive Technology in 2000.Application In Synthesis of 2-Ethylhexyl benzoate The following contents are mentioned in the article:

Plastisol viscosity reduction and control is an important property specification in many vinyl plastisol formulations. 2-Ethylhexyl benzoate plasticizer is under development that functions as a viscosity reducer for PVC. It also is a highly solvating plasticizer in standard plastisol systems. Data are presented on the effects of the new benzoate plasticizer on the properties of phthalate- and benzoate-containing plastisols and vinyl sheet for flooring. This study involved multiple reactions and reactants, such as 2-Ethylhexyl benzoate (cas: 5444-75-7Application In Synthesis of 2-Ethylhexyl benzoate).

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. 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.Application In Synthesis of 2-Ethylhexyl benzoate

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

Guzzo, Peter R. et al. published their research in Journal of Organic Chemistry in 2003 | CAS: 500353-15-1

tert-Butyl 2,4-difluorobenzoate (cas: 500353-15-1) 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. 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.Formula: C11H12F2O2

Preparation of 8-Amido-2-Dimethylamino-1,2,3,4-Tetrahydro-2-Dibenzofurans and Several Fluorinated Derivatives via [3,3]-Sigmatropic Rearrangement of O-Aryloximes was written by Guzzo, Peter R.;Buckle, Ronald N.;Chou, Ming;Dinn, Sean R.;Flaugh, Michael E.;Kiefer, Anton D. Jr.;Ryter, Kendal T.;Sampognaro, Anthony J.;Tregay, Steven W.;Xu, Yao-Chang. And the article was included in Journal of Organic Chemistry in 2003.Formula: C11H12F2O2 The following contents are mentioned in the article:

Methodol. to prepare 8-amido-2-amino-1,2,3,4-tetrahydro-2-dibenzofurans, analogs with a fluorine substituent incorporated in the 6-, 7-, and 9-positions, and a 6,9-difluorinated analog is described. The tetrahydrodibenzofuran ring systems are prepared by acid-catalyzed [3,3]-sigmatropic rearrangement of O-aryloximes. Regioselective reactions to prepare the requisite O-aryloxime intermediates from com. available fluorobenzene derivatives are discussed. This study involved multiple reactions and reactants, such as tert-Butyl 2,4-difluorobenzoate (cas: 500353-15-1Formula: C11H12F2O2).

tert-Butyl 2,4-difluorobenzoate (cas: 500353-15-1) 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. 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.Formula: C11H12F2O2

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

Hayashi, Toshio et al. published their research in Tetrahedron Letters in 1983 | CAS: 50767-78-7

(E)-Dodeca-9,11-dien-1-yl acetate (cas: 50767-78-7) belongs to esters. Carboxylic acid esters of low molecular weight are colourless, volatile liquids with pleasant odours, slightly soluble in water. 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: (E)-Dodeca-9,11-dien-1-yl acetate

A highly stereo- and regioselective synthesis of (E)-1,3-dienes and (E,E)-1,3,5-trienes was written by Hayashi, Toshio;Yanagida, Masako;Matsuda, Yuko;Oishi, Takeshi. And the article was included in Tetrahedron Letters in 1983.Recommanded Product: (E)-Dodeca-9,11-dien-1-yl acetate The following contents are mentioned in the article:

(E)-1,3-Dodecadien-1-yl acetate, an insect sex pheromone of the red bollworm moth, and (E,E)-1,3,5-undecatriene, a component of Dictyopteris and Galbanum, were synthesized in a highly stereo- and regioselective manner from allyl and pentadienyl dithiocarbamates, resp., by α-alkylation, rearrangement to the γ-alkyl derivative, reaction with Me3SiCH2I, and oxidative desulfurization. This study involved multiple reactions and reactants, such as (E)-Dodeca-9,11-dien-1-yl acetate (cas: 50767-78-7Recommanded Product: (E)-Dodeca-9,11-dien-1-yl acetate).

(E)-Dodeca-9,11-dien-1-yl acetate (cas: 50767-78-7) belongs to esters. Carboxylic acid esters of low molecular weight are colourless, volatile liquids with pleasant odours, slightly soluble in water. 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: (E)-Dodeca-9,11-dien-1-yl acetate

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

Yearick, Kimberly et al. published their research in Organic Letters in 2008 | CAS: 898787-14-9

Ethyl 4-(2,2,2-Trifluoroacetyl)benzoate (cas: 898787-14-9) 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. 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.Computed Properties of C11H9F3O3

Catalytic Enantioselective Addition of Diethylzinc to Trifluoromethyl Ketones was written by Yearick, Kimberly;Wolf, Christian. And the article was included in Organic Letters in 2008.Computed Properties of C11H9F3O3 The following contents are mentioned in the article:

A procedure for nucleophilic addition of diethylzinc to trifluoromethyl ketones was developed. The TMEDA-catalyzed method converts aromatic substrates to the corresponding 2-aryl-1,1,1-trifluorobutan-2-ols in up to 99% yield, and it is also applicable to less reactive aliphatic ketones if stoichiometric ligand amounts are employed. The first asym. variant producing tertiary alcs. with up to 61% ee when TBOX is used as catalyst is described. This study involved multiple reactions and reactants, such as Ethyl 4-(2,2,2-Trifluoroacetyl)benzoate (cas: 898787-14-9Computed Properties of C11H9F3O3).

Ethyl 4-(2,2,2-Trifluoroacetyl)benzoate (cas: 898787-14-9) 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. 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.Computed Properties of C11H9F3O3

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

Semenova, Anna M. et al. published their research in Mendeleev Communications in 2021 | CAS: 102-09-0

Diphenyl carbonate (cas: 102-09-0) 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. 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.Recommanded Product: Diphenyl carbonate

Phosgene-free synthesis of symmetric bis(polyfluoroalkyl) carbonates was written by Semenova, Anna M.;Ezhikova, Marina A.;Kodess, Mikhail I.;Zapevalov, Aleksandr Ya.;Pestov, Aleksandr V.. And the article was included in Mendeleev Communications in 2021.Recommanded Product: Diphenyl carbonate The following contents are mentioned in the article:

A phosgene-free synthesis of sym. bis(polyfluoroalkyl) carbonates H(CF2CF2)nCH2OC(O)COCH2(CF2CF2)nH (n = 1, 2, 3) involves the transesterification of di-Ph carbonate with polyfluoroalkanols H(CF2CF2)nCH2OH promoted by stoichiometric amounts of titanium(iv) alkoxides Ti(OR)4 (R = Et, n-Bu, i-Pr). This study involved multiple reactions and reactants, such as Diphenyl carbonate (cas: 102-09-0Recommanded Product: Diphenyl carbonate).

Diphenyl carbonate (cas: 102-09-0) 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. 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.Recommanded Product: Diphenyl carbonate

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

Orita, Akihiro et al. published their research in Angewandte Chemie, International Edition in English in 1997 | CAS: 37905-02-5

(2E,6E)-3,7-Dimethyl-8-oxoocta-2,6-dien-1-yl acetate (cas: 37905-02-5) 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. 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: C12H18O3

Integrated chemical process: an extremely concise synthesis of vitamin A was written by Orita, Akihiro;Yamashita, Yasuo;Toh, Akiji;Otera, Junzo. And the article was included in Angewandte Chemie, International Edition in English in 1997.Formula: C12H18O3 The following contents are mentioned in the article:

A one-pot procedure conducted stepwise under basic conditions gave an improved yield via an integrated chem. process. Lithium salt of a cyclogeranylsulfone treated with a dimethyloctadienal gave the addition product I which was converted to the MOM ether, underwent double elimination when exposed to MeOK to yield vitamin A. Addition of cyclohexane as a cosolvent in the elimination step increased the yield slightly. This study involved multiple reactions and reactants, such as (2E,6E)-3,7-Dimethyl-8-oxoocta-2,6-dien-1-yl acetate (cas: 37905-02-5Formula: C12H18O3).

(2E,6E)-3,7-Dimethyl-8-oxoocta-2,6-dien-1-yl acetate (cas: 37905-02-5) 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. 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: C12H18O3

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

Minigulov, F. G. et al. published their research in Plasticheskie Massy in 2020 | CAS: 102-09-0

Diphenyl carbonate (cas: 102-09-0) belongs to esters. Carboxylic acid esters of low molecular weight are colourless, volatile liquids with pleasant odours, slightly soluble in water. 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.COA of Formula: C13H10O3

Some features of the environmentally friendly “phosgene-free” polycarbonate production technology was written by Minigulov, F. G.;Presnyakov, V. V.;Shigabutdinov, A. K.;Safin, D. Kh.;Presnyakov, A. V.;Valitov, A. R.;Safin, A. F.. And the article was included in Plasticheskie Massy in 2020.COA of Formula: C13H10O3 The following contents are mentioned in the article:

Environmental safety of the phosgene-free production of polycarbonate in comparison with the processes based on the use of phosgene was studied. Historical stages of development of this technol. and the main technol. solutions ensuring its effectiveness were reviewed. The advantages of the phosgene-free technol. were demonstrated using the example of Kazanorgsintez PJSC. The main characteristics of the polycarbonates are presented. This study involved multiple reactions and reactants, such as Diphenyl carbonate (cas: 102-09-0COA of Formula: C13H10O3).

Diphenyl carbonate (cas: 102-09-0) belongs to esters. Carboxylic acid esters of low molecular weight are colourless, volatile liquids with pleasant odours, slightly soluble in water. 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.COA of Formula: C13H10O3

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

Zhang, Peng et al. published their research in Journal of Organic Chemistry in 2012 | CAS: 898787-14-9

Ethyl 4-(2,2,2-Trifluoroacetyl)benzoate (cas: 898787-14-9) 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. 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.Quality Control of Ethyl 4-(2,2,2-Trifluoroacetyl)benzoate

Synthesis of Pentafluorinated β-Hydroxy Ketones was written by Zhang, Peng;Wolf, Christian. And the article was included in Journal of Organic Chemistry in 2012.Quality Control of Ethyl 4-(2,2,2-Trifluoroacetyl)benzoate The following contents are mentioned in the article:

The LHMDS-promoted in situ generation of difluoroenolates from readily available 1-aryl and 1-alkyl 2,2,4,4,4-pentafluorobutan-1,3-dione hydrates has been used to produce a series of pentafluorinated β-hydroxy ketones in up to 95% yield. The reaction proceeds under mild conditions, tolerates a wide range of functional groups, and is complete within 10 min. Reduction toward the corresponding 1,3-diol with DIBAL gives quant. amounts and favors the formation of the syn-isomer. This study involved multiple reactions and reactants, such as Ethyl 4-(2,2,2-Trifluoroacetyl)benzoate (cas: 898787-14-9Quality Control of Ethyl 4-(2,2,2-Trifluoroacetyl)benzoate).

Ethyl 4-(2,2,2-Trifluoroacetyl)benzoate (cas: 898787-14-9) 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. 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.Quality Control of Ethyl 4-(2,2,2-Trifluoroacetyl)benzoate

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

Lester, Ralph et al. published their research in Journal of Chromatography in 1980 | CAS: 50767-78-7

(E)-Dodeca-9,11-dien-1-yl acetate (cas: 50767-78-7) 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 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.Quality Control of (E)-Dodeca-9,11-dien-1-yl acetate

4-(p-Methoxycinnamyloxy)-4′-methoxyazobenzene: a nematic liquid crystal for the gas-liquid chromatographic analysis of the stereochemistry of lepidopterous sex pheromones and related unsaturated fatty alcohols and derivatives was written by Lester, Ralph;Hall, David R.. And the article was included in Journal of Chromatography in 1980.Quality Control of (E)-Dodeca-9,11-dien-1-yl acetate The following contents are mentioned in the article:

A study of the gas chromatog. behavior of unsaturated fatty alcs. and acetates on a nematic liquid crystal, 4-(p-methoxycinnamyloxy)-4′-methoxyazobenzene, as stationary phase showed that excellent separations of isomers are possible within the nematic and supercooled temperature limits of this compound Separations of isomers of some mono- and di-unsaturated insect pheromones are given to illustrate the selectivity of this liquid crystal towards olefinic isomers. This study involved multiple reactions and reactants, such as (E)-Dodeca-9,11-dien-1-yl acetate (cas: 50767-78-7Quality Control of (E)-Dodeca-9,11-dien-1-yl acetate).

(E)-Dodeca-9,11-dien-1-yl acetate (cas: 50767-78-7) 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 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.Quality Control of (E)-Dodeca-9,11-dien-1-yl acetate

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

Lee, Hyung Kook et al. published their research in Bioorganic & Medicinal Chemistry Letters in 2008 | CAS: 1061284-70-5

Methyl 2-(4-bromophenyl)-3-methylbutanoate (cas: 1061284-70-5) 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. 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.Name: Methyl 2-(4-bromophenyl)-3-methylbutanoate

Synthesis and evaluation of α,α’-disubstituted phenylacetate derivatives for T-type calcium channel blockers was written by Lee, Hyung Kook;Lee, Yun Suk;Roh, Eun Joo;Rhim, Hyewhon;Lee, Jae Yeol;Shin, Kye Jung. And the article was included in Bioorganic & Medicinal Chemistry Letters in 2008.Name: Methyl 2-(4-bromophenyl)-3-methylbutanoate The following contents are mentioned in the article:

A number of α,α’-disubstituted phenylacetate derivatives were synthesized and evaluated as T-type calcium channel blockers. Among them, compound I (IC50 = 8.17 ± 0.48 nM) showed the most potent T-type calcium current blocking activity and higher potency than Mibefradil (IC50 = 1.34 ± 0.49 μM). The pharmacokinetic profile and subtype selectivity over L-type calcium channel were satisfied for further animal assay using disease model. This study involved multiple reactions and reactants, such as Methyl 2-(4-bromophenyl)-3-methylbutanoate (cas: 1061284-70-5Name: Methyl 2-(4-bromophenyl)-3-methylbutanoate).

Methyl 2-(4-bromophenyl)-3-methylbutanoate (cas: 1061284-70-5) 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. 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.Name: Methyl 2-(4-bromophenyl)-3-methylbutanoate

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