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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
Structure of ISOPROPENYL ACETATE

SMILES

CC(=C)OC(C)=O

InChI

InChIKey=HETCEOQFVDFGSY-UHFFFAOYSA-N
InChI=1S/C5H8O2/c1-4(2)7-5(3)6/h1H2,2-3H3

HIDE SMILES / InChI

Approval Year

PubMed

PubMed

TitleDatePubMed
Lipase-catalyzed irreversible transesterification of 1-(2-furyl)ethanol using isopropenyl acetate.
2001 Feb
Efficient lipase-catalyzed enantioselective desymmetrization of prochiral 2,2-disubstituted 1,3-propanediols and meso 1,2-diols using 1-ethoxyvinyl 2-furoate.
2002 Jan 25
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 Nov
One-Pot synthesis of gamma,delta-unsaturated carbonyl compounds from allyl alcohols and vinyl or isopropenyl acetates catalyzed by [IrCl(cod)]2.
2006 Aug 4
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 Jan 15
Dynamic kinetic resolution of secondary alcohols combining enzyme-catalyzed transesterification and zeolite-catalyzed racemization.
2007
Air-stable racemization catalysts for the dynamic kinetic resolution of secondary alcohols.
2007 Aug 31
Large-scale ruthenium- and enzyme-catalyzed dynamic kinetic resolution of (rac)-1-phenylethanol.
2007 Dec 20
Enol esters: versatile substrates for Mannich-type multicomponent reactions.
2007 Oct 11
The allosteric modulation of lipases and its possible biological relevance.
2007 Sep 7
Inhibitory effect of some acetyl esters and acetamides on glycation of the histone H1.
2008 Jul-Aug
Large nonstatistical branching ratio in the dissociation of pentane-2,4-dione radical cation: an ab initio direct classical trajectory study.
2009 Feb 26
Patents
Name Type Language
ISOPROPENYL ACETATE
MI  
Systematic Name English
1-PROPEN-2-OL, ACETATE [HSDB]
Common Name English
1-PROPEN-2-YL ACETATE
Systematic Name English
ISOPROPENYL ACETATE [MI]
Common Name English
FEMA NO. 4152
Code English
1-PROPEN-2-OL 2-ACETATE
Common Name English
NSC-2197
Code English
Code System Code Type Description
JECFA MONOGRAPH
1813
Created by admin on Fri Dec 15 19:12:14 GMT 2023 , Edited by admin on Fri Dec 15 19:12:14 GMT 2023
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PUBCHEM
7916
Created by admin on Fri Dec 15 19:12:14 GMT 2023 , Edited by admin on Fri Dec 15 19:12:14 GMT 2023
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CAS
108-22-5
Created by admin on Fri Dec 15 19:12:14 GMT 2023 , Edited by admin on Fri Dec 15 19:12:14 GMT 2023
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WIKIPEDIA
Isopropenyl acetate
Created by admin on Fri Dec 15 19:12:14 GMT 2023 , Edited by admin on Fri Dec 15 19:12:14 GMT 2023
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EPA CompTox
DTXSID3031492
Created by admin on Fri Dec 15 19:12:14 GMT 2023 , Edited by admin on Fri Dec 15 19:12:14 GMT 2023
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MERCK INDEX
m6519
Created by admin on Fri Dec 15 19:12:14 GMT 2023 , Edited by admin on Fri Dec 15 19:12:14 GMT 2023
PRIMARY Merck Index
MESH
C555950
Created by admin on Fri Dec 15 19:12:14 GMT 2023 , Edited by admin on Fri Dec 15 19:12:14 GMT 2023
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ECHA (EC/EINECS)
203-562-7
Created by admin on Fri Dec 15 19:12:14 GMT 2023 , Edited by admin on Fri Dec 15 19:12:14 GMT 2023
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FDA UNII
4AR9LAS337
Created by admin on Fri Dec 15 19:12:14 GMT 2023 , Edited by admin on Fri Dec 15 19:12:14 GMT 2023
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NSC
2197
Created by admin on Fri Dec 15 19:12:14 GMT 2023 , Edited by admin on Fri Dec 15 19:12:14 GMT 2023
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HSDB
5383
Created by admin on Fri Dec 15 19:12:14 GMT 2023 , Edited by admin on Fri Dec 15 19:12:14 GMT 2023
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