应用
Reactant for synthesis of oxazino[4,3-a]indoles via cascade addition-cyclization reactions, reactant for preparation of indolecarboxamides as cannabinoid CB1 receptor antagonists, reactant for preparation of indole-3-propionic acids as antiinflammatory and analgesic agents, reactant for Friedel-Crafts acylation with nitrobenzoyl chloride. Indole ring system is an important building block or intermediate in the synthesis of many pharmaceutical agents. It is formed during the Fischer indolization of ethyl pyruvate 2-[2-(methanesulfonyloxy)-4-methyl]phenylhydrazine. ?? Reactant for oximation reactions

备注
Store away from strong oxidizing agents. Keep container tightly closed. Store in cool, dry conditions in well sealed containers.

基本信息

MDL
MFCD00022703

分子式
C₁₂H₁₃NO₂

分子量
203.24

熔点
161-165°

沸点
236°/4mm

灵敏度
Ambient temperatures.

形态
Solid

溶解性
Soluble in methanol, and dichloromethane. Insoluble in water.

Beilstein
159437

安全信息

安全等级
22-24/25
Do not breathe dust.Avoid contact with skin and eyes.

TSCA
否