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Merck
CN

523364

Sigma-Aldrich

2-溴-3-硝基吡啶

98%

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About This Item

经验公式(希尔记法):
C5H3BrN2O2
CAS号:
分子量:
202.99
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22

方案

98%

表单

solid

mp

122-125 °C (lit.)

官能团

bromo
nitro

SMILES字符串

[O-][N+](=O)c1cccnc1Br

InChI

1S/C5H3BrN2O2/c6-5-4(8(9)10)2-1-3-7-5/h1-3H

InChI key

ZCCUFLITCDHRMG-UHFFFAOYSA-N

一般描述

2-Bromo-3-nitropyridine is a pyridine derivative. It can be synthesized from 3-nitropyridine-2-amine.

应用

2-Bromo-3-nitropyridine may be used in the synthesis of the following:
  • 3-nitropyridine-2-carbonitrile
  • pyrrolo[3,2-b]pyridine
  • 3-(hetero)arylated phenothiazines
  • 7-anilino-6-azaindole-1-benznesulfonamides

象形图

Exclamation mark

警示用语:

Warning

危险声明

危险分类

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

靶器官

Respiratory system

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

dust mask type N95 (US), Eyeshields, Gloves

法规信息

新产品

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分析证书(COA)

Lot/Batch Number

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访问文档库

Synthesis and Electronic Properties of 3-Acceptor-Substituted and 3, 7-Bisacceptor-Substituted Phenothiazines.
Sailer M, et al.
European Journal of Organic Chemistry, 2006(2), 423-435 (2006)
Condensed heteroaromatic ring systems. XII. Synthesis of indole derivatives from ethyl 2-bromocarbanilates.
Sakamoto T, et al.
Chemical & Pharmaceutical Bulletin, 35(5), 1823-1828 (1987)
Yvonnick Loidreau et al.
European journal of medicinal chemistry, 58, 171-183 (2012-11-06)
A useful and rapid access to libraries of N-arylbenzo[b]thieno[3,2-d]pyrimidin-4-amines and their pyrido and pyrazino analogues was designed and optimized for the first time via microwave-accelerated condensation and Dimroth rearrangement of the starting anilines with N'-(2-cyanoaryl)-N,N-dimethylformimidamides obtained by reaction of thiophene
Hsueh-Yun Lee et al.
Journal of medicinal chemistry, 56(20), 8008-8018 (2013-10-11)
Preliminary biological data on 7-anilino-6-azaindoles (8-11) suggested that hydrophobic substituents at C7 contribute to enhancement of antiproliferative activity. A novel series of 7-aryl-6-azaindole-1-benzenesulfonamides (12-22) were developed and showed improved cytotoxicity compared to ABT751 (5). The conversion of C7 phenyl rings

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