117188
2-Hydroxy-4-nitrobenzoic acid
97%
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About This Item
Linear Formula:
HOC6H3(NO2)CO2H
CAS Number:
Molecular Weight:
183.12
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
210-584-0
MDL number:
Product Name
2-Hydroxy-4-nitrobenzoic acid, 97%
InChI key
UKWUOTZGXIZAJC-UHFFFAOYSA-N
InChI
1S/C7H5NO5/c9-6-3-4(8(12)13)1-2-5(6)7(10)11/h1-3,9H,(H,10,11)
SMILES string
OC(=O)c1ccc(cc1O)[N+]([O-])=O
assay
97%
mp
235-239 °C (lit.)
functional group
carboxylic acid
nitro
Quality Level
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General description
2-Hydroxy-4-nitrobenzoic acid is metabolized to 2,4-dihydroxybenzoic acid (2,4-DHBA) by a mono-oxygenase with the concomitant release of chloride and nitrite ions.
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
Regulatory Information
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Novel pathway for the degradation of 2-chloro-4-nitrobenzoic acid by Acinetobacter sp. strain RKJ12.
Dhan Prakash et al.
Applied and environmental microbiology, 77(18), 6606-6613 (2011-08-02)
The organism Acinetobacter sp. RKJ12 is capable of utilizing 2-chloro-4-nitrobenzoic acid (2C4NBA) as a sole source of carbon, nitrogen, and energy. In the degradation of 2C4NBA by strain RKJ12, various metabolites were isolated and identified by a combination of chromatographic
Behnoush Hajian et al.
Cell chemical biology, 26(6), 781-791 (2019-04-02)
The folate biosynthetic pathway offers many druggable targets that have yet to be exploited in tuberculosis therapy. Herein, we have identified a series of small molecules that interrupt Mycobacterium tuberculosis (Mtb) folate metabolism by dual targeting of dihydrofolate reductase (DHFR), a
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