产品名称

英文名称：N-Phenylhydroxylamine

同义词

J-000193、N-phenyl hydroxylamine、UNII-282MU82Z9A、A800252、NSC 223099、AMY18021、NSC-223099、beta-Phenylhydroxylamine、Hydroxylamine, N-phenyl-、N-PHENYLHYDROXYLAMINE、N-Phenyl-hydroxylamine、.beta.-Phenylhydroxylamine、N-hydroxylaniline、phenyl hydroxylamine、PHENYLH、N-羟基苯胺

产品性质

CAS编号：100-65-2

分子式：C6H7NO

分子量：109.13

EC号：202-875-6

MDL号：MFCD00045718

PubChem编号：7518

别名：N-羟基苯胺

英文别名：J-000193|N-phenyl hydroxylamine|UNII-282MU82Z9A|A800252|NSC 223099|AMY18021|NSC-223099|beta-Phenylhydroxylamine|Hydroxylamine, N-phenyl-|N-PHENYLHYDROXYLAMINE|N-Phenyl-hydroxylamine|.beta.-Phenylhydroxylamine|N-hydroxylaniline|phenyl hydroxylamine|PHENYLH

规格或纯度：≥98.0% (HPLC)

英文名称：N-Phenylhydroxylamine

储存温度：避光,-20°C储存,充氩

运输条件：超低温冰袋运输

产品介绍：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 reactionIntroductionN-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.ApplicationN-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

IUPAC Name：N-phenylhydroxylamine

INCHI：InChI=1S/C6H7NO/c8-7-6-4-2-1-3-5-6/h1-5,7-8H

InChi Key：CKRZKMFTZCFYGB-UHFFFAOYSA-N

Canonical SMILES：C1=CC=C(C=C1)NO

Isomeric SMILES：C1=CC=C(C=C1)NO

WGK Germany：3

RTECS：NC4900000

PubChem CID：7518

UN Number：2811

Packing Group：I

敏感性：对光线敏感

熔点：80-84℃

象形图：

信号词：Danger

危险声明：H301 Toxic if swallowed

预防措施声明：P321,P405,P501,P264,P270,P330,P301+P316

Class：6.1

个人防护装备：Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges

产品包装