质量水平
方案
≥95.0%
表单
solid
mp
80-84 °C
储存温度
−20°C
SMILES字符串
ONc1ccccc1
InChI
1S/C6H7NO/c8-7-6-4-2-1-3-5-6/h1-5,7-8H
InChI key
CKRZKMFTZCFYGB-UHFFFAOYSA-N
应用
N-苯基羟胺作为起始材料，可用于下列合成反应：
- 通过连续3,3-重排和环脱水反应，用金催化剂与脂肪族末端炔烃进行处理，合成2-烷基吲哚。
- 通过三组分一锅催化法，与醛和 α, β不饱和醛合成异恶唑烷。
- 通过homo3+2偶极环加成反应，处理醛和环丙烷，合成四氢1,2-恶嗪。
警示用语：
Danger
危险声明
预防措施声明
危险分类
Acute Tox. 3 Oral
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, Faceshields, Gloves, type P2 (EN 143) respirator cartridges
历史批次信息供参考:
分析证书(COA)
Lot/Batch Number
T P Bradshaw et al.
Free radical biology & medicine, 18(2), 279-285 (1995-02-01)
Previous studies have shown that incubation of rat red blood cells in vitro with phenylhydroxylamine (50-300 microM) induces rapid splenic sequestration of the red cells on reintroduction to isologous rats. EPR and the spin trapping agent, 5,5-dimethyl-1-pyrroline-N-oxide (DMPO), were utilized
Nilanjana Chowdhury et al.
Bioorganic & medicinal chemistry letters, 20(18), 5414-5417 (2010-08-21)
Photoinduced homolytic fission of nitrogen-oxygen bond in N,O-diacyl-4-benzoyl-N-phenylhydroxylamines using 310 nm UV light for 10 min produced acylaminyl and acyloxy radicals, which resulted in single strand cleavage of DNA at pH 7.0. Further the DNA cleaving ability of N,O-diacyl-4-benzoyl-N-phenylhydroxylamines found
Copper-catalyzed amination of alkenes and ketones by phenylhydroxylamine.
Ho C-M and Lau T-C
New. J. Chem., 24(11), 859-863 (2000)
Au-catalyzed synthesis of 2-alkylindoles from N-arylhydroxylamines and terminal alkynes
Wang Y, et al.
Chemical Communications (Cambridge, England), 47(27), 7815-7817 (2011)
Magnesium iodide promoted reactions of nitrones with cyclopropanes: a synthesis of tetrahydro-1, 2-oxazines.
Ganton M D and Kerr M A
The Journal of Organic Chemistry, 69(24), 8554-8557 (2004)
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