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Details

Stereochemistry ACHIRAL
Molecular Formula C7H4Cl2O2
Molecular Weight 191.011
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 2,4-DICHLOROBENZOIC ACID

SMILES

OC(=O)C1=CC=C(Cl)C=C1Cl

InChI

InChIKey=ATCRIUVQKHMXSH-UHFFFAOYSA-N
InChI=1S/C7H4Cl2O2/c8-4-1-2-5(7(10)11)6(9)3-4/h1-3H,(H,10,11)

HIDE SMILES / InChI

Molecular Formula C7H4Cl2O2
Molecular Weight 191.011
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Inhibition of Pneumocystis carinii dihydropteroate synthetase by para-acetamidobenzoic acid: possible mechanism of action of isoprinosine in human immunodeficiency virus infection.
1993 Jun
Induction of the halobenzoate catabolic pathway and cometabolism of ortho-chlorobenzoates in Pseudomonas aeruginosa 142 grown on glucose-supplemented media.
2001
Halogenated organic contaminants in sediments of the Havel and Spree rivers (Germany). Part 5 of organic compounds as contaminants of the Elbe river and its tributaries.
2001 Oct 15
Automated dynamic liquid-liquid-liquid microextraction followed by high-performance liquid chromatography-ultraviolet detection for the determination of phenoxy acid herbicides in environmental waters.
2005 Aug 5
Ambigol C and 2,4-dichlorobenzoic acid, natural products produced by the terrestrial cyanobacterium Fischerella ambigua.
2005 Mar
Expression profiling of drug response--from genes to pathways.
2006
2-(1H-1,2,3-Benzotriazol-1-yl)-1-(4-ethyl-benzo-yl)ethyl 2,4-dichloro-benzoate.
2008 Apr 30
A genome-wide survey for host response of silkworm, Bombyx mori during pathogen Bacillus bombyseptieus infection.
2009 Dec 1
New polymeric composites based on poly(-caprolactone) and layered double hydroxides containing antimicrobial species.
2009 Mar
Design of a novel nucleoside analog as potent inhibitor of the NAD dependent deacetylase, SIRT2.
2010 Dec
Synthesis of some new pyrimido[2',1':2,3]thiazolo[4,5-b]quinoxaline derivatives as anti-inflammatory and analgesic agents.
2010 May
Patents
Substance Class Chemical
Created
by admin
on Fri Dec 15 19:01:07 GMT 2023
Edited
by admin
on Fri Dec 15 19:01:07 GMT 2023
Record UNII
0SR0320D45
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
2,4-DICHLOROBENZOIC ACID
Systematic Name English
NSC-578
Code English
FUROSEMIDE IMPURITY E [EP IMPURITY]
Common Name English
BENZOIC ACID, 2,4-DICHLORO-
Common Name English
DICHLOROBENZOIC ACID, 2,4-
Common Name English
Code System Code Type Description
EPA CompTox
DTXSID0024977
Created by admin on Fri Dec 15 19:01:07 GMT 2023 , Edited by admin on Fri Dec 15 19:01:07 GMT 2023
PRIMARY
PUBCHEM
5787
Created by admin on Fri Dec 15 19:01:07 GMT 2023 , Edited by admin on Fri Dec 15 19:01:07 GMT 2023
PRIMARY
CHEBI
30748
Created by admin on Fri Dec 15 19:01:07 GMT 2023 , Edited by admin on Fri Dec 15 19:01:07 GMT 2023
PRIMARY
NSC
578
Created by admin on Fri Dec 15 19:01:07 GMT 2023 , Edited by admin on Fri Dec 15 19:01:07 GMT 2023
PRIMARY
FDA UNII
0SR0320D45
Created by admin on Fri Dec 15 19:01:07 GMT 2023 , Edited by admin on Fri Dec 15 19:01:07 GMT 2023
PRIMARY
CAS
50-84-0
Created by admin on Fri Dec 15 19:01:07 GMT 2023 , Edited by admin on Fri Dec 15 19:01:07 GMT 2023
PRIMARY
ECHA (EC/EINECS)
200-067-8
Created by admin on Fri Dec 15 19:01:07 GMT 2023 , Edited by admin on Fri Dec 15 19:01:07 GMT 2023
PRIMARY
Related Record Type Details
PARENT -> IMPURITY
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP