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Merck
CN

262226

1-溴-2,4-二硝基苯

97%

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线性分子式:
BrC6H3(NO2)2
化学文摘社编号:
分子量:
247.00
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
209-539-8
MDL number:
Assay:
97%
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InChI key

PBOPJYORIDJAFE-UHFFFAOYSA-N

InChI

1S/C6H3BrN2O4/c7-5-2-1-4(8(10)11)3-6(5)9(12)13/h1-3H

SMILES string

[O-][N+](=O)c1ccc(Br)c(c1)[N+]([O-])=O

assay

97%

mp

71-73 °C (lit.)

functional group

bromo, nitro

Quality Level

Application

使用了 1-溴-2,4-二硝基苯:
  • KO 2 冠醚配合物处理苯制备 2,4-二硝基苯酚的研究
  • 鸡和大鼠前列腺素 D 2 合成酶 (PGDS) 的蛋白质测定和谷胱甘肽 S-转移酶 (GST) 测定的底物

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - Skin Sens. 1

存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Faceshields, Gloves

法规信息

危险化学品
此项目有

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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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)
Nucleophilic radical aromatic substituion with superoxide ion.
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
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
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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