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Details

Stereochemistry ACHIRAL
Molecular Formula C6H10O2
Molecular Weight 114.1424
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 1
Charge 0

SHOW SMILES / InChI
Structure of 2-HEXENOIC ACID, (2E)-

SMILES

CCC\C=C\C(O)=O

InChI

InChIKey=NIONDZDPPYHYKY-SNAWJCMRSA-N
InChI=1S/C6H10O2/c1-2-3-4-5-6(7)8/h4-5H,2-3H2,1H3,(H,7,8)/b5-4+

HIDE SMILES / InChI

Approval Year

PubMed

PubMed

TitleDatePubMed
Composition of the volatiles from intact and mechanically pierced tea aphid-tea shoot complexes and their attraction to natural enemies of the tea aphid.
2002 Apr 24
Behavioral and electrophysiological responses of natural enemies to synomones from tea shoots and kairomones from tea aphids, Toxoptera aurantii.
2002 Nov
Synthesis, molecular modeling, and evaluation of nonphenolic indole analogs of mycophenolic acid.
2004 Jun 1
Synthesis of some monocyclic analogues of mycophenolic acid via the Johnson ortho ester Claisen rearrangement.
2005 Dec 1
Metabolite fingerprinting in transgenic Nicotiana tabacum altered by the Escherichia coli glutamate dehydrogenase gene.
2005 Jun 30
Interspecific pheromone cross-attraction among soybean bugs (Heteroptera): does Piezodorus hybneri (Pentatomidae) utilize the pheromone of Riptortus clavatus (Alydidae) as a kairomone?
2006 Jul
Olfactory sensitivity through the course of psychosis: Relationships to olfactory identification, symptomatology and the schizophrenia odour.
2007 Jan 15
FaGT2: a multifunctional enzyme from strawberry (Fragaria x ananassa) fruits involved in the metabolism of natural and xenobiotic compounds.
2007 Jul
Influence of Honey on the Suppression of Human Low Density Lipoprotein (LDL) Peroxidation (In vitro).
2009 Mar
Pheromonal cross-attraction in true bugs (Heteroptera): attraction of Piezodorus hybneri (Pentatomidae) to its pheromone versus the pheromone of Riptortus pedestris (Alydidae).
2010 Dec
Odorant-binding proteins of the malaria mosquito Anopheles funestus sensu stricto.
2010 Oct 22
Differential expression pattern of an acidic 9/13-lipoxygenase in flower opening and senescence and in leaf response to phloem feeders in the tea plant.
2010 Oct 25
Name Type Language
2-HEXENOIC ACID, (2E)-
Common Name English
2-HEXENOIC ACID, TRANS-
Common Name English
TRANS-2-HEXENOIC ACID
FHFI  
Systematic Name English
2-HEXENOIC ACID, (E)-
Common Name English
TRANS-HEX-2-ENOIC ACID
Systematic Name English
TRANS-2-HEXENOIC ACID [FHFI]
Common Name English
(E)-2-HEXENOIC ACID
Systematic Name English
FEMA NO. 3169
Code English
HEXENOIC ACID, TRANS 2-
Common Name English
Classification Tree Code System Code
JECFA EVALUATION TRANS-2-HEXENOIC ACID
Created by admin on Fri Dec 15 16:52:42 GMT 2023 , Edited by admin on Fri Dec 15 16:52:42 GMT 2023
Code System Code Type Description
FDA UNII
VQ24908VRU
Created by admin on Fri Dec 15 16:52:42 GMT 2023 , Edited by admin on Fri Dec 15 16:52:42 GMT 2023
PRIMARY
EPA CompTox
DTXSID60884601
Created by admin on Fri Dec 15 16:52:42 GMT 2023 , Edited by admin on Fri Dec 15 16:52:42 GMT 2023
PRIMARY
CHEBI
87721
Created by admin on Fri Dec 15 16:52:42 GMT 2023 , Edited by admin on Fri Dec 15 16:52:42 GMT 2023
PRIMARY
JECFA MONOGRAPH
1360
Created by admin on Fri Dec 15 16:52:42 GMT 2023 , Edited by admin on Fri Dec 15 16:52:42 GMT 2023
PRIMARY
CAS
13419-69-7
Created by admin on Fri Dec 15 16:52:42 GMT 2023 , Edited by admin on Fri Dec 15 16:52:42 GMT 2023
PRIMARY
PUBCHEM
5282707
Created by admin on Fri Dec 15 16:52:42 GMT 2023 , Edited by admin on Fri Dec 15 16:52:42 GMT 2023
PRIMARY
ECHA (EC/EINECS)
236-528-5
Created by admin on Fri Dec 15 16:52:42 GMT 2023 , Edited by admin on Fri Dec 15 16:52:42 GMT 2023
PRIMARY