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About This Item
Linear Formula:
BrC6H3(NO2)2
CAS Number:
Molecular Weight:
247.00
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
Quality Level
assay
97%
mp
71-73 °C (lit.)
SMILES string
[O-][N+](=O)c1ccc(Br)c(c1)[N+]([O-])=O
InChI
1S/C6H3BrN2O4/c7-5-2-1-4(8(10)11)3-6(5)9(12)13/h1-3H
InChI key
PBOPJYORIDJAFE-UHFFFAOYSA-N
Related Categories
Application
1-Bromo-2,4-dinitrobenzene has been used:
- in the preparation of 2,4-dinitrophenol via treatment with KO2-crown ether complex in benzene
- as substrate in protein determination and glutathione S-transferase (GST) assay of chicken and rat prostaglandin D2 synthase (PGDS)
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - Skin Sens. 1
wgk_germany
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
Certificates of Analysis (COA)
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Frimer A and Rosenthal I.
Tetrahedron Letters, 17(32), 2809-2812 (1976)
K C Chen et al.
Drug and chemical toxicology, 3(3), 305-318 (1980-01-01)
The formation of glutathione (GSH) conjugate in the detoxification of [Ring-UL-14C]-2,4-dinitrobromobenzene (DNBB) was investigated using rat liver cytosolic fraction. The mercapturic acid conjugate in rats was also studied by collection of urine of rats dosed with radioactive DNBB by intraperitoneal
The reaction of poly-L-ornithine with 1-halo-2,4-dinitrobenzenes.
R C Parker et al.
The International journal of biochemistry, 13(4), 513-516 (1981-01-01)
A M Thomson et al.
The Biochemical journal, 333 ( Pt 2), 317-325 (1998-07-11)
The Expressed Sequence Tag database has been screened for cDNA clones encoding prostaglandin D2 synthases (PGDSs) by using a BLAST search with the N-terminal amino acid sequence of rat GSH-dependent PGDS, a class Sigma glutathione S-transferase (GST). This resulted in
R L Gupta et al.
Mutation research, 381(1), 41-47 (1997-12-24)
The 1-halogen substituted 2,4-dinitrobenzenes have been found to be mutagenic in Salmonella TA98 with an activity order of 1-fluoro > 1-chloro > 1-bromo > 1-iodo. This specific activity was not lowered in the nitroreductase deficient strain TA98NR and O-acetyltransferase deficient
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