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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 4-PENTENOIC ACID

SMILES

OC(=O)CCC=C

InChI

InChIKey=HVAMZGADVCBITI-UHFFFAOYSA-N
InChI=1S/C5H8O2/c1-2-3-4-5(6)7/h2H,1,3-4H2,(H,6,7)

HIDE SMILES / InChI

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

PubMed

TitleDatePubMed
Production of functionalized polyhydroxyalkanoates by genetically modified Methylobacterium extorquens strains.
2010-09-16
Extension of the PNA world by functionalized PNA monomers eligible candidates for inverse Diels Alder Click Chemistry.
2010-06-27
Pentenoic acid pathways for cellulosic biofuels.
2010-06-14
Formulations of valproate alter valproate metabolism: a single oral dose kinetic study.
2009-10
Gold(I)-catalyzed coupling reactions for the synthesis of diverse small molecules using the build/couple/pair strategy.
2009-04-22
(S)-2-acetoxy-5-undecanone, female sex pheromone of the raspberry cane midge, Resseliella theobaldi (Barnes).
2009-02
Caenorhabditis elegans F09E10.3 encodes a putative 3-oxoacyl-thioester reductase of mitochondrial type 2 fatty acid synthase FASII that is functional in yeast.
2009
Total synthesis of (-)-talaumidin and (-)-galbelgin.
2009
A xerogel-sequestered selenoxide catalyst for brominations with hydrogen peroxide and sodium bromide in an aqueous environment.
2008-09-05
Bimetallic dendrimer-encapsulated nanoparticles as catalysts: a review of the research advances.
2008-08
Temperature, pH, and ionic strength induced changes of the swelling behavior of PNIPAM-poly(allylacetic acid) copolymer microgels.
2008-06-17
Alternative pig liver esterase (APLE) - cloning, identification and functional expression in Pichia pastoris of a versatile new biocatalyst.
2008-02-01
Part 3. Triethylborane-air: a suitable initiator for intermolecular radical additions of S-2-oxoalkyl-thionocarbonates (S-xanthates) to olefins.
2007-12-13
Part 2. Mechanistic aspects of the reduction of S-alkyl-thionocarbonates in the presence of triethylborane and air.
2007-12-12
Effect of silimarin, succinic acid, and their combination on bioenergetics of the brain in experimental encephalopathy.
2007-12
Presence of thiamine pyrophosphate in mammalian peroxisomes.
2007-06-27
[Effects of silymarin and its combination with succinic acid on brain bioenergetics in rats with experimental inhibition of beta-oxidation of fatty acids].
2007-05-26
Diglucosyl-glycerolipids from the marine sponge-associated Bacillus pumilus strain AAS3: their production, enzymatic modification and properties.
2004-05
Use of a low-density microarray for studying gene expression patterns induced by hepatotoxicants on primary cultures of rat hepatocytes.
2003-10
Glucose binding to molecularly imprinted polymers.
2002
Photoinduced, ionic Meerwein arylation of olefins.
2001-09-21
Fluorinated analogues as mechanistic probes in valproic acid hepatotoxicity: hepatic microvesicular steatosis and glutathione status.
1995-07-01
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:47:02 GMT 2025
Edited
by admin
on Mon Mar 31 18:47:02 GMT 2025
Record UNII
D4S77Y29FB
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
FEMA NO. 2843
Preferred Name English
4-PENTENOIC ACID
FHFI  
Systematic Name English
NSC-9000
Code English
4-PENTENOIC ACID [FHFI]
Common Name English
NSC-20944
Code English
ALLYLACETIC ACID
Systematic Name English
Classification Tree Code System Code
JECFA EVALUATION 4-PENTENOIC ACID
Created by admin on Mon Mar 31 18:47:02 GMT 2025 , Edited by admin on Mon Mar 31 18:47:02 GMT 2025
CFR 21 CFR 172.515
Created by admin on Mon Mar 31 18:47:02 GMT 2025 , Edited by admin on Mon Mar 31 18:47:02 GMT 2025
Code System Code Type Description
EVMPD
SUB176894
Created by admin on Mon Mar 31 18:47:02 GMT 2025 , Edited by admin on Mon Mar 31 18:47:02 GMT 2025
PRIMARY
JECFA MONOGRAPH
378
Created by admin on Mon Mar 31 18:47:02 GMT 2025 , Edited by admin on Mon Mar 31 18:47:02 GMT 2025
PRIMARY
SMS_ID
100000162877
Created by admin on Mon Mar 31 18:47:02 GMT 2025 , Edited by admin on Mon Mar 31 18:47:02 GMT 2025
PRIMARY
EPA CompTox
DTXSID0044448
Created by admin on Mon Mar 31 18:47:02 GMT 2025 , Edited by admin on Mon Mar 31 18:47:02 GMT 2025
PRIMARY
CAS
591-80-0
Created by admin on Mon Mar 31 18:47:02 GMT 2025 , Edited by admin on Mon Mar 31 18:47:02 GMT 2025
PRIMARY
PUBCHEM
61138
Created by admin on Mon Mar 31 18:47:02 GMT 2025 , Edited by admin on Mon Mar 31 18:47:02 GMT 2025
PRIMARY
MESH
C009785
Created by admin on Mon Mar 31 18:47:02 GMT 2025 , Edited by admin on Mon Mar 31 18:47:02 GMT 2025
PRIMARY
CHEBI
35936
Created by admin on Mon Mar 31 18:47:02 GMT 2025 , Edited by admin on Mon Mar 31 18:47:02 GMT 2025
PRIMARY
NSC
20944
Created by admin on Mon Mar 31 18:47:02 GMT 2025 , Edited by admin on Mon Mar 31 18:47:02 GMT 2025
PRIMARY
FDA UNII
D4S77Y29FB
Created by admin on Mon Mar 31 18:47:02 GMT 2025 , Edited by admin on Mon Mar 31 18:47:02 GMT 2025
PRIMARY
ECHA (EC/EINECS)
209-732-7
Created by admin on Mon Mar 31 18:47:02 GMT 2025 , Edited by admin on Mon Mar 31 18:47:02 GMT 2025
PRIMARY
NSC
9000
Created by admin on Mon Mar 31 18:47:02 GMT 2025 , Edited by admin on Mon Mar 31 18:47:02 GMT 2025
PRIMARY