139572
2,4-Dichlorobenzoic acid
98%
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About This Item
Linear Formula:
Cl2C6H3CO2H
CAS Number:
Molecular Weight:
191.01
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
200-067-8
Beilstein/REAXYS Number:
1868192
MDL number:
Assay:
98%
Quality Level
assay
98%
mp
157-160 °C (lit.)
solubility
ethanol: soluble 1 g/10 mL, clear, colorless
functional group
carboxylic acid, chloro
SMILES string
OC(=O)c1ccc(Cl)cc1Cl
InChI
1S/C7H4Cl2O2/c8-4-1-2-5(7(10)11)6(9)3-4/h1-3H,(H,10,11)
InChI key
ATCRIUVQKHMXSH-UHFFFAOYSA-N
General description
2,4-Dichlorobenzoic acid is the degradation product of chlorfenvinphos in water treated by photo-fenton driven by solar irradiation.
Application
2,4-Dichlorobenzoic acid was used in solid-phase extraction and gas chromatographic determination of polar acidic herbicides in surface water. It was used as reagent during the synthesis of pyrimido[2′,1′:2,3]thiazolo[4,5-b]quinoxaline derivatives. It was used as starting reagent during the synthesis of 1-(substituted)-1,4-dihydro-6-nitro-4-oxo-7-(sub-secondary amino)-quinoline-3-carboxylic acids.
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signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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Gas chromatographic determination of acid herbicides in surface water samples with electron-capture detection and mass spectrometric confirmation.
Vink M and Van der Poll JM.
Journal of Chromatography A, 733(1), 361-366 (1996)
Palaniappan Senthilkumar et al.
European journal of medicinal chemistry, 44(1), 345-358 (2008-05-27)
Various 1-(substituted)-1,4-dihydro-6-nitro-4-oxo-7-(sub-secondary amino)-quinoline-3-carboxylic acids were synthesized from 2,4-dichlorobenzoic acid by six step synthesis. The compounds were evaluated for antimycobacterial in vitro and in vivo against Mycobacterium tuberculosis H37Rv (MTB), multi-drug resistant Mycobacterium tuberculosis (MDR-TB) and Mycobacterium smegmatis (MC(2)) and also
A Iu Sokolov et al.
Eksperimental'naia i klinicheskaia farmakologiia, 74(5), 13-16 (2011-08-04)
Neurophysiological experiments on anesthetized rats were used to study the effects of various doses (12.5, 25, 37.5 mg/kg, i.v.) of drug composition migrepin (representing a combination of potassium-2,4-dichlorobenzoate, carbamazepine, and caffeine) on background firing of the trigeminal nucleus caudalis neurons
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 139572-100G | 04061838732903 |
| 139572-5G | 04061831828344 |