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 |
|---|---|---|
| Design of a novel nucleoside analog as potent inhibitor of the NAD dependent deacetylase, SIRT2. | 2010-12 |
|
| Synthesis of some new pyrimido[2',1':2,3]thiazolo[4,5-b]quinoxaline derivatives as anti-inflammatory and analgesic agents. | 2010-05 |
|
| Hydrogen-bonded supramolecular motifs in pyrimethaminium 4-methylbenzoate, pyrimethaminium 3-hydroxypicolinate and pyrimethaminium 2,4-dichlorobenzoate. | 2010-03 |
|
| A genome-wide survey for host response of silkworm, Bombyx mori during pathogen Bacillus bombyseptieus infection. | 2009-12-01 |
|
| Formation of chlorinated disinfection by-products in viticulture. | 2009-07 |
|
| New polymeric composites based on poly(-caprolactone) and layered double hydroxides containing antimicrobial species. | 2009-03 |
|
| Synthesis and antimycobacterial activities of novel 6-nitroquinolone-3-carboxylic acids. | 2009-01 |
|
| Synthesis, antimycobacterial activities and phototoxic evaluation of 5H-thiazolo[3,2-a]quinoline-4-carboxylic acid derivatives. | 2008-09 |
|
| 2-(1H-1,2,3-Benzotriazol-1-yl)-1-(4-ethyl-benzo-yl)ethyl 2,4-dichloro-benzoate. | 2008-04-30 |
|
| Metabolic peculiarities of Aspergillus niger disclosed by comparative metabolic genomics. | 2007 |
|
| Injection port derivatization following ion-pair hollow fiber-protected liquid-phase microextraction for determining acidic herbicides by gas chromatography/mass spectrometry. | 2006-10-15 |
|
| Effects of cyanobacterium Fischerella ambigua isolates and cell free culture media on zebrafish (Danio rerio) embryo development. | 2006-10 |
|
| Expression profiling of drug response--from genes to pathways. | 2006 |
|
| Photosensitizing properties of 2,4-dichlorobenzoic acid and chlorinated biphenyl carboxylic acids, potentially key components of chromophoric dissolved organic matter. | 2005-08-28 |
|
| Automated dynamic liquid-liquid-liquid microextraction followed by high-performance liquid chromatography-ultraviolet detection for the determination of phenoxy acid herbicides in environmental waters. | 2005-08-05 |
|
| Ambigol C and 2,4-dichlorobenzoic acid, natural products produced by the terrestrial cyanobacterium Fischerella ambigua. | 2005-03 |
|
| Structure elucidation and characterization of polychlorinated biphenyl carboxylic acids as major constituents of chromophoric dissolved organic matter in seawater. | 2004-10-15 |
|
| 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. | 2001-10-15 |
|
| Induction of the halobenzoate catabolic pathway and cometabolism of ortho-chlorobenzoates in Pseudomonas aeruginosa 142 grown on glucose-supplemented media. | 2001 |
|
| Inhibition of Pneumocystis carinii dihydropteroate synthetase by para-acetamidobenzoic acid: possible mechanism of action of isoprinosine in human immunodeficiency virus infection. | 1993-06 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 19:30:19 GMT 2025
by
admin
on
Mon Mar 31 19:30:19 GMT 2025
|
| Record UNII |
0SR0320D45
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
Download
| Name | Type | Language | ||
|---|---|---|---|---|
|
Preferred Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English |
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
DTXSID0024977
Created by
admin on Mon Mar 31 19:30:19 GMT 2025 , Edited by admin on Mon Mar 31 19:30:19 GMT 2025
|
PRIMARY | |||
|
5787
Created by
admin on Mon Mar 31 19:30:19 GMT 2025 , Edited by admin on Mon Mar 31 19:30:19 GMT 2025
|
PRIMARY | |||
|
30748
Created by
admin on Mon Mar 31 19:30:19 GMT 2025 , Edited by admin on Mon Mar 31 19:30:19 GMT 2025
|
PRIMARY | |||
|
578
Created by
admin on Mon Mar 31 19:30:19 GMT 2025 , Edited by admin on Mon Mar 31 19:30:19 GMT 2025
|
PRIMARY | |||
|
0SR0320D45
Created by
admin on Mon Mar 31 19:30:19 GMT 2025 , Edited by admin on Mon Mar 31 19:30:19 GMT 2025
|
PRIMARY | |||
|
50-84-0
Created by
admin on Mon Mar 31 19:30:19 GMT 2025 , Edited by admin on Mon Mar 31 19:30:19 GMT 2025
|
PRIMARY | |||
|
200-067-8
Created by
admin on Mon Mar 31 19:30:19 GMT 2025 , Edited by admin on Mon Mar 31 19:30:19 GMT 2025
|
PRIMARY |
| Related Record | Type | Details | ||
|---|---|---|---|---|
|
PARENT -> IMPURITY |
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
|
