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
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)
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
Title | Date | PubMed |
---|---|---|
Inhibition of Pneumocystis carinii dihydropteroate synthetase by para-acetamidobenzoic acid: possible mechanism of action of isoprinosine in human immunodeficiency virus infection. | 1993 Jun |
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Induction of the halobenzoate catabolic pathway and cometabolism of ortho-chlorobenzoates in Pseudomonas aeruginosa 142 grown on glucose-supplemented media. | 2001 |
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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 |
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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 |
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Ambigol C and 2,4-dichlorobenzoic acid, natural products produced by the terrestrial cyanobacterium Fischerella ambigua. | 2005 Mar |
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Expression profiling of drug response--from genes to pathways. | 2006 |
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2-(1H-1,2,3-Benzotriazol-1-yl)-1-(4-ethyl-benzo-yl)ethyl 2,4-dichloro-benzoate. | 2008 Apr 30 |
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A genome-wide survey for host response of silkworm, Bombyx mori during pathogen Bacillus bombyseptieus infection. | 2009 Dec 1 |
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New polymeric composites based on poly(-caprolactone) and layered double hydroxides containing antimicrobial species. | 2009 Mar |
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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 |
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 19:01:07 GMT 2023
by
admin
on
Fri Dec 15 19:01:07 GMT 2023
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Record UNII |
0SR0320D45
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Record Status |
Validated (UNII)
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Record Version |
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200-067-8
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