262226
1-Bromo-2,4-dinitrobenzene
97%
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About This Item
Productos recomendados
Quality Level
assay
97%
mp
71-73 °C (lit.)
functional group
bromo
nitro
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
Categorías relacionadas
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
Storage Class
11 - Combustible Solids
wgk_germany
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
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Los clientes también vieron
The reaction of poly-L-ornithine with 1-halo-2,4-dinitrobenzenes.
The International journal of biochemistry, 13(4), 513-516 (1981-01-01)
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.
Tetrahedron Letters, 17(32), 2809-2812 (1976)
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
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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