All Photos(1)
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)
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - Skin Sens. 1
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
危险化学品
Certificates of Analysis (COA)
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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
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
Nucleophilic radical aromatic substituion with superoxide ion.
Frimer A and Rosenthal I.
Tetrahedron Letters, 17(32), 2809-2812 (1976)
E M Gagan et al.
Archives of environmental contamination and toxicology, 52(3), 283-293 (2007-01-27)
Frequently the toxicity of an organic chemical mixture is close to dose-additive, even when the agents are thought to induce toxicity at different molecular sites of action. These findings appear to conflict with the hypothesis that a strictly dose-additive combined
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