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Merck
CN

521744

Sigma-Aldrich

2-氨基-6-溴吡啶

98%

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About This Item

经验公式(希尔记法):
C5H5BrN2
CAS号:
分子量:
173.01
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22

质量水平

方案

98%

mp

88-91 °C (lit.)

官能团

bromo

SMILES字符串

Nc1cccc(Br)n1

InChI

1S/C5H5BrN2/c6-4-2-1-3-5(7)8-4/h1-3H,(H2,7,8)

InChI key

BKLJUYPLUWUEOQ-UHFFFAOYSA-N

一般描述

从表氯醇合成了 2-氨基-6-溴吡啶。

应用

2-氨基-6-溴吡啶可用于以下物质的合成:
  • 2-氨基-6-二乙基氨基吡啶
  • 2,6-二-(甲基氨基)吡啶
  • 3-(6-溴吡啶-2-基)-2-(2,6-二氟苯基)-1,3-噻唑烷-4-酮
  • N-(6-溴吡啶-2-基)十二烷基酰胺
  • 2-溴-6-碘吡啶
用于合成抗 HIV 试剂。
用于高效一锅法合成 7-氮杂吲哚。

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


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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访问文档库

Microwave-assisted synthesis of benzimidazole and thiazolidinone derivatives as HIV-1 RT inhibitors.
Rao A, et al.
ARKIVOC (Gainesville, FL, United States), 147, 155-155 (2004)
Maria Letizia Barreca et al.
Farmaco (Societa chimica italiana : 1989), 58(3), 259-263 (2003-03-07)
This paper reports our work in the field of nonnucleoside RT inhibitors (NNRTIs). On the basis of extensive studies on 1H,3H-thiazolo[3,4-a]benzimidazole derivatives (TBZs) followed by structure-activity relationship (SAR) considerations and molecular modeling, the design and synthesis of a series of
Masato Ikeda et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 11(2), 662-668 (2004-11-27)
The bow-shaped molecule 1 bearing a self-complementary DAAD-ADDA (D=donor A=acceptor) hydrogen-bonding array generates, in hydrocarbon solvents, highly ordered supramolecular sheet aggregates that subsequently give rise to gels by formation of an entangled network. The process of hierarchical self-assembly of compound
Synthesis of ?Acetylene-Expanded? Tridentate Ligands
Holmes BT, et al.
Molecules (Basel), 7(5), 447-455 (2002)
II. Derivatives of 2, 6-Diaminopyridine1.
Bernstein J, et al.
Journal of the American Chemical Society, 69(5), 1151-1115 (1947)

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