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
CC(=C)OC(C)=O
InChI
InChIKey=HETCEOQFVDFGSY-UHFFFAOYSA-N
InChI=1S/C5H8O2/c1-4(2)7-5(3)6/h1H2,2-3H3
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Large nonstatistical branching ratio in the dissociation of pentane-2,4-dione radical cation: an ab initio direct classical trajectory study. | 2009-02-26 |
|
| Inhibitory effect of some acetyl esters and acetamides on glycation of the histone H1. | 2008-09-25 |
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| Large-scale ruthenium- and enzyme-catalyzed dynamic kinetic resolution of (rac)-1-phenylethanol. | 2007-12-20 |
|
| Enol esters: versatile substrates for Mannich-type multicomponent reactions. | 2007-10-11 |
|
| The allosteric modulation of lipases and its possible biological relevance. | 2007-09-07 |
|
| Air-stable racemization catalysts for the dynamic kinetic resolution of secondary alcohols. | 2007-08-31 |
|
| Dynamic kinetic resolution of secondary alcohols combining enzyme-catalyzed transesterification and zeolite-catalyzed racemization. | 2007 |
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| One-Pot synthesis of gamma,delta-unsaturated carbonyl compounds from allyl alcohols and vinyl or isopropenyl acetates catalyzed by [IrCl(cod)]2. | 2006-08-04 |
|
| Application and comparison of immobilized and coated amylose tris-(3,5-dimethylphenylcarbamate) chiral stationary phases for the enantioselective separation of beta-blockers enantiomers by liquid chromatography. | 2006-01-15 |
|
| Stereochemistry of a diastereoisomeric amphiphile and the species of the lipase influence enzyme activity in the transesterification catalyzed by a lipase-co-lyophilizate with the amphiphile in organic media. | 2003-11 |
|
| Efficient lipase-catalyzed enantioselective desymmetrization of prochiral 2,2-disubstituted 1,3-propanediols and meso 1,2-diols using 1-ethoxyvinyl 2-furoate. | 2002-01-25 |
|
| Lipase-catalyzed irreversible transesterification of 1-(2-furyl)ethanol using isopropenyl acetate. | 2001-02 |
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Code | English |
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1813
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7916
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108-22-5
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Isopropenyl acetate
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DTXSID3031492
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m6519
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C555950
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203-562-7
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4AR9LAS337
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2197
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5383
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SUBSTANCE RECORD