推荐产品
表单
solid
质量水平
mp
123-126 °C (lit.)
SMILES字符串
N(Nc1ccccc1)c2ccccc2
InChI
1S/C12H12N2/c1-3-7-11(8-4-1)13-14-12-9-5-2-6-10-12/h1-10,13-14H
InChI key
YBQZXXMEJHZYMB-UHFFFAOYSA-N
正在寻找类似产品? 访问 产品对比指南
一般描述
氢化偶氮苯是氧化偶氮苯氢化成苯胺的中间体。
通过在 THF 中用 SmI（2）还原偶氮苯来制备氢化偶氮苯。
应用
作为以下反应的反应物：
- 与有机金属钽配合物发生的插入反应
- 三氯化钛（III）催化的还原反应，生成胺
- 研究苯重排的机理
- 与 N-杂环稳定的甲硅烷基发生的反应
- 二锰酰胺酰肼簇合物的合成
- 铁介导的肼还原反应，生成亚芳基铁立方烷
其他说明
含有不定量的偶氮苯
警示用语：
Danger
危险声明
危险分类
Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Carc. 1B
储存分类代码
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
Eyeshields, Gloves, type P3 (EN 143) respirator cartridges
法规信息
监管及禁止进口产品
Chintada Nageswara Rao et al.
The Journal of organic chemistry, 76(22), 9438-9443 (2011-10-19)
The reduction of azobenzene by SmI(2) in THF to give hydrazobenzene was investigated. The kinetics are first order in the substrate and first order in SmI(2). The kinetic order in MeOH is ca. 0.56, and in TFE it is ca.
H Fabre et al.
Journal of pharmaceutical sciences, 73(12), 1706-1709 (1984-12-01)
A high-performance liquid chromatographic method was developed for the simultaneous determination of azobenzene, hydrazobenzene, and four other decomposition products in phenylbutazone injectable formulations. Separation was achieved on a C18 column, with 0.1 M Tris-citrate buffer (pH 5.25) and acetonitrile (52:48)
Darol E Dodd et al.
International journal of toxicology, 31(6), 564-571 (2012-11-09)
Male F344 rats were exposed to hydrazobenzene (HZB) by dietary feed at concentrations of 0, 5, 20, 80, 200, or 300 ppm for 5 days, 2 weeks, 4 weeks, or 13 weeks duration. End points evaluated included clinical observations, body
Hydrazobenzene.
Report on carcinogens : carcinogen profiles, 10, 139-140 (2004-08-26)
Waseem Ahmed et al.
Journal of enzyme inhibition and medicinal chemistry, 25(5), 673-678 (2010-01-13)
Virtual screening of an in-house virtual library of synthetic compounds using FlexX, followed by enzyme inhibition, identified hydrazide and hydrazine derivatives as novel aspartic protease inhibitors. These compounds inhibited human cathepsin D and Plasmodium falciparum plasmepsin-II with low micromolar concentrations
我们的科学家团队拥有各种研究领域经验，包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.
联系技术服务部门