| 产品名称 | N-苯基羟胺 |
|---|---|
| 英文名称 | N-Phenylhydroxylamine |
| 别名 | N-羟基苯胺 |
| 英文别名 | N-Hydroxybenzenamine |
| 应用 | A useful synthetic intermediate |
| 规格或纯度 | ≥98.0% (HPLC) |
| 运输条件 | 超低温冰袋运输 |
介绍
N-Phenylhydroxylamine is a useful synthetic intermediate. It was used as a reagent to prepare 6-halo-2-amino-3-formylchromones as potential topoisomerase inhibitor anticancer agents. It was also used in the synthesis of N-(chlorophenyl)cycloalkyl-hydroxamic acids and N-phenyl-N-hydroxycyclohexylacetamide with anti-viral activities.
用途
N-Phenylhydroxylamine can be used as a starting material for the synthesis of:
· 2-alkylindoles by treating with aliphatic terminal alkynes using gold catalyst via sequential 3,3-rearrangements and cyclodehydrations.
· Isoxazolidines by reacting with aldehydes and α, β-unsaturated aldehydes via a three-component one-pot catalytic reaction.
· Tetrahydro-1,2-oxazines by treating with an aldehyde and cyclopropane via homo 3+2 dipolar cycloaddition reaction
Introduction
N-Phenylhydroxylamine is a useful synthetic intermediate. It was used as a reagent to prepare 6-halo-2-amino-3-formylchromones as potential topoisomerase inhibitor anticancer agents. It was also used in the synthesis of N-(chlorophenyl)cycloalkyl-hydroxamic acids and N-phenyl-N-hydroxycyclohexylacetamide with anti-viral activities.
Application
N-Phenylhydroxylamine can be used as a starting material for the synthesis of:
· 2-alkylindoles by treating with aliphatic terminal alkynes using gold catalyst via sequential 3,3-rearrangements and cyclodehydrations.
· Isoxazolidines by reacting with aldehydes and α, β-unsaturated aldehydes via a three-component one-pot catalytic reaction.
· Tetrahydro-1,2-oxazines by treating with an aldehyde and cyclopropane via homo 3+2 dipolar cycloaddition reaction
| CAS编号 | 100-65-2 |
|---|---|
| 敏感性 | 对光线敏感 |
| 熔点 | 80-84℃ |
| 储存温度 | 避光,-20°C储存,充氩 |
| RTECS | NC4900000 |
| MDL号 | MFCD00045718 |
| 分子量 | 109.13 |
| 分子式 | C6H7NO |
| EC号 | 202-875-6 |
| 品牌 | 阿拉丁 |
| PubChem CID | 7518 |