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Details

Stereochemistry RACEMIC
Molecular Formula C3H5ClO2
Molecular Weight 108.524
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 2-CHLOROPROPIONIC ACID

SMILES

CC(Cl)C(O)=O

InChI

InChIKey=GAWAYYRQGQZKCR-UHFFFAOYSA-N
InChI=1S/C3H5ClO2/c1-2(4)3(5)6/h2H,1H3,(H,5,6)

HIDE SMILES / InChI

Approval Year

PubMed

PubMed

TitleDatePubMed
L-2-chloropropionic acid-induced cerebellar granule cell necrosis is potentiated by L-type calcium channel antagonists.
1997
Use of structure-activity relationships for probing biochemical mechanisms: glutathione transferase zeta conjugation of haloacids.
2001
Toxic effect of L-2-chloropropionate on cultured rat cerebellar granule cells is ameliorated after inhibition of reactive oxygen species formation.
2001 Dec 1
Re-evaluation of archival material for neuronal cell injury produced by L-2-chloropropionic acid in the rat brain.
2004 Dec
Putrescine as a marker of the effects of 2-chloropropionic acid in the rat brain.
2004 May 27
Genetic organization of the dhlA gene encoding 1,2-dichloroethane dechlorinase from Xanthobacter flavus UE15.
2004 Sep
Copper(II)-mediated resolution of alpha-halo carboxylic acids with chiral O,O'-dibenzoyltartaric acid: spontaneous racemization and crystallization-induced dynamic resolution.
2005 Dec 7
Synthesis of a peroxime proliferator activated receptor (PPAR) alpha/gamma agonist via stereocontrolled Williamson ether synthesis and stereospecific SN2 reaction of S-2-chloro propionic acid with phenoxides.
2005 Jun 10
Purification, crystallization and preliminary crystallographic analysis of DehIVa, a dehalogenase from Burkholderia cepacia MBA4.
2005 Mar 1
Synthesis of PPAR agonist via asymmetric hydrogenation of a cinnamic acid derivative and stereospecific displacement of (S)-2-chloropropionic acid.
2005 May 12
2-Haloacrylate reductase, a novel enzyme of the medium chain dehydrogenase/reductase superfamily that catalyzes the reduction of a carbon-carbon double bond of unsaturated organohalogen compounds.
2005 May 27
Biochemical and molecular characterisation of the 2,3-dichloro-1-propanol dehalogenase and stereospecific haloalkanoic dehalogenases from a versatile Agrobacterium sp.
2005 Oct
Thermoresponsive comb-shaped copolymer-Si(100) hybrids for accelerated temperature-dependent cell detachment.
2006 Mar
Production of (S)-2-chloropropionate by asymmetric reduction of 2-chloroacrylate with 2-haloacrylate reductase coupled with glucose dehydrogenase.
2008 Apr
Tuning the chiral cavity of macrocyclic receptor for chiral recognition and discrimination.
2008 Nov 21
Roles of K151 and D180 in L-2-haloacid dehalogenase from Pseudomonas sp. YL: analysis by molecular dynamics and ab initio fragment molecular orbital calculations.
2009 Dec
Direct determination of the enantiomeric purity or enantiomeric composition of methylpropionates using a single capacitive microsensor.
2009 Mar 1
Clinical physiology and mechanism of dizocilpine (MK-801): electron transfer, radicals, redox metabolites and bioactivity.
2010 Jan-Feb
Role of pyruvate dehydrogenase kinase 4 in regulation of blood glucose levels.
2010 Oct
Patents
Name Type Language
2-CHLOROPROPIONIC ACID
Systematic Name English
PROPIONIC ACID, .ALPHA.-CHLORO-
Common Name English
(±)-2-CHLOROPROPIONIC ACID
Systematic Name English
2-CHLOROPROPANOIC ACID
Systematic Name English
.ALPHA.-CHLOROPROPIONIC ACID
Systematic Name English
NSC-173
Code English
(RS)-2-CHLOROPROPANOIC ACID
Systematic Name English
.ALPHA.-CHLOROPROPIONIC ACID, (±)-
Common Name English
PROPANOIC ACID, 2-CHLORO-
Common Name English
(±)-2-CHLOROPROPANOIC ACID
Systematic Name English
.ALPHA.-MONOCHLOROPROPIONIC ACID
Systematic Name English
2-Chloropropanoic acid [WHO-DD]
Common Name English
PROPIONIC ACID, 2-CHLORO-
Common Name English
(±)-.ALPHA.-CHLOROPROPANOIC ACID
Systematic Name English
(RS)-2-CHLOROPROPIONIC ACID
Systematic Name English
Code System Code Type Description
WIKIPEDIA
2-CHLOROPROPIONIC ACID
Created by admin on Sat Dec 16 01:28:40 GMT 2023 , Edited by admin on Sat Dec 16 01:28:40 GMT 2023
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MESH
C021974
Created by admin on Sat Dec 16 01:28:40 GMT 2023 , Edited by admin on Sat Dec 16 01:28:40 GMT 2023
PRIMARY
ECHA (EC/EINECS)
209-952-3
Created by admin on Sat Dec 16 01:28:40 GMT 2023 , Edited by admin on Sat Dec 16 01:28:40 GMT 2023
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FDA UNII
ADV1WUE1NB
Created by admin on Sat Dec 16 01:28:40 GMT 2023 , Edited by admin on Sat Dec 16 01:28:40 GMT 2023
PRIMARY
EPA CompTox
DTXSID0021545
Created by admin on Sat Dec 16 01:28:40 GMT 2023 , Edited by admin on Sat Dec 16 01:28:40 GMT 2023
PRIMARY
NSC
173
Created by admin on Sat Dec 16 01:28:40 GMT 2023 , Edited by admin on Sat Dec 16 01:28:40 GMT 2023
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PUBCHEM
11734
Created by admin on Sat Dec 16 01:28:40 GMT 2023 , Edited by admin on Sat Dec 16 01:28:40 GMT 2023
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HSDB
5713
Created by admin on Sat Dec 16 01:28:40 GMT 2023 , Edited by admin on Sat Dec 16 01:28:40 GMT 2023
PRIMARY
CAS
598-78-7
Created by admin on Sat Dec 16 01:28:40 GMT 2023 , Edited by admin on Sat Dec 16 01:28:40 GMT 2023
PRIMARY