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6-羟基吲哚_分子结构_CAS_2380-86-1)
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6-羟基吲哚

产品号 18805 公司名称 Sigma Aldrich
CAS号 2380-86-1 公司网站 http://www.sigmaaldrich.com
分子式 C8H7NO 电 话 1-800-521-8956
分子量 133.14728 传 真
纯 度 ≥99.0% (GC) 电子邮件
保 存 Chembase数据库ID: 10444

产品价格信息

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产品别名

标题
6-Hydroxyindole
IUPAC标准名
1H-indol-6-ol
IUPAC传统名
1H-indol-6-ol
别名
6-Indolol
吲哚醇

产品登记号

CAS号 2380-86-1
EC号 417-020-4
MDL号 MFCD00152101

产品性质

欧盟危险性物质标志 有害性(Harmful) 有害性(Harmful) (Xn)
欧盟危险性物质标志 环境危害性(Nature polluting) 环境危害性(Nature polluting) (N)
MSDS下载 下载链接
个人保护装置 dust mask type N95 (US), Eyeshields, Faceshields, Gloves
GHS警示性声明 P273-P280-P305 + P351 + P338
RID/ADR UN 3077 9/PG 3
危险公开号 22-41-43-51/53
安全公开号 24-26-37/39-61
联合国危险货物等级 9
联合国危险货物编号 3077
联合国危险货物包装类别(PG) 3
德国WGK号 2
GHS危险品标识 GHS05
GHS危险品标识 GHS07
GHS危险品标识 GHS09
GHS警示词 Danger
GHS危险声明 H302-H317-H318-H411
Empirical Formula (Hill Notation) C8H7NO
纯度 ≥99.0% (GC)
熔点 125-128 °C

产品详细信息

详细说明 (English)
Packaging
1 g in glass bottle
Application

• Reactant for preparation of tryptophan dioxygenase inhibitors pyridyl-ethenyl-indoles as potential anticancer immunomodulators1
• Reactant for asymmetrical synthesis of notoamide J as a potential biosynthetic precursor of prenylated indole alkaloids2
• Reactant for preparation of (quinolinyloxymethyl)isoxazolecarboxylate esters antituberculosis agents3
• Reactant for preparation of indolyl(propanolamine) derivatives as HIV inhibitors4
• Reactant for preparation of indoleoxyacetic acid derivatives as peroxisome proliferator-activated receptor agonists5
• Reactant for preparation of 1-aroylindole 3-aroylindoles combretastatin A-4 analogs as antitumor agents and tubulin polymerization inhibitors6
详细说明 (简体中文)
包装
1 g in glass bottle
Application

• Reactant for preparation of tryptophan dioxygenase inhibitors pyridyl-ethenyl-indoles as potential anticancer immunomodulators1
• Reactant for asymmetrical synthesis of notoamide J as a potential biosynthetic precursor of prenylated indole alkaloids2
• Reactant for preparation of (quinolinyloxymethyl)isoxazolecarboxylate esters antituberculosis agents3
• Reactant for preparation of indolyl(propanolamine) derivatives as HIV inhibitors4
• Reactant for preparation of indoleoxyacetic acid derivatives as peroxisome proliferator-activated receptor agonists5
• Reactant for preparation of 1-aroylindole 3-aroylindoles combretastatin A-4 analogs as antitumor agents and tubulin polymerization inhibitors6

参考文献