Details
Stereochemistry | ACHIRAL |
Molecular Formula | C5H8O2 |
Molecular Weight | 100.1158 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
CCC(=O)OC=C
InChI
InChIKey=UIWXSTHGICQLQT-UHFFFAOYSA-N
InChI=1S/C5H8O2/c1-3-5(6)7-4-2/h4H,2-3H2,1H3
Molecular Formula | C5H8O2 |
Molecular Weight | 100.1158 |
Charge | 0 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
Approval Year
PubMed
Title | Date | PubMed |
---|---|---|
Activation of pig liver esterase in organic media with organic polymers: application to the enantioselective acylation of racemic functionalized secondary alcohols. | 2001 May 18 |
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Lipase-catalysed hydrolysis of short-chain substrates in solution and in emulsion: a kinetic study. | 2001 Nov 30 |
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Distinction between esterases and lipases: a kinetic study with vinyl esters and TAG. | 2002 Jul |
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Kinetic resolution of rac-2-pentanol catalyzed by Candida antarctica lipase B in the ionic liquid, 1-butyl-3-methylimidazolium bis[(trifluoromethyl)sulfonyl]amide. | 2004 Feb |
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Biochemical and molecular characterization of a lipase produced by Rhizopus oryzae. | 2006 Jul |
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Markedly improving Novozym 435-mediated regioselective acylation of 1-beta-D-arabinofuranosylcytosine by using co-solvent mixtures as the reaction media. | 2006 Jul 25 |
|
Purification and biochemical characterization of a turkey preduodenal esterase. | 2006 Nov-Dec |
|
Non-lipolytic and lipolytic sequence-related carboxylesterases: a comparative study of the structure-function relationships of rabbit liver esterase 1 and bovine pancreatic bile-salt-activated lipase. | 2010 Nov |
Patents
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 20:03:49 GMT 2023
by
admin
on
Fri Dec 15 20:03:49 GMT 2023
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Record UNII |
2437OJ3190
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Record Status |
Validated (UNII)
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Record Version |
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5275
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Vinyl propionate
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203-293-5
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7750
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DTXSID9051537
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2437OJ3190
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105-38-4
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