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1-甲基吲哚-3-甲酸_分子结构_CAS_32387-21-6)
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1-甲基吲哚-3-甲酸

产品号 465313 公司名称 Sigma Aldrich
CAS号 32387-21-6 公司网站 http://www.sigmaaldrich.com
分子式 C10H9NO2 电 话 1-800-521-8956
分子量 175.18396 传 真
纯 度 97% 电子邮件
保 存 Chembase数据库ID: 59679

产品价格信息

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产品别名

标题
1-Methylindole-3-carboxylic acid
IUPAC标准名
1-methyl-1H-indole-3-carboxylic acid
IUPAC传统名
1-methylindole-3-carboxylic acid

产品登记号

CAS号 32387-21-6
PubChem SID 24870267
MDL号 MFCD01321244

产品性质

Empirical Formula (Hill Notation) C10H9NO2
纯度 97%
熔点 197-200 °C (dec.)(lit.)
GHS危险品标识 GHS07
GHS警示词 Warning
GHS危险声明 H315-H319-H335
欧盟危险性物质标志 刺激性(Irritant) 刺激性(Irritant) (Xi)
MSDS下载 下载链接
个人保护装置 dust mask type N95 (US), Eyeshields, Gloves
GHS警示性声明 P261-P305 + P351 + P338
危险公开号 36/37/38
安全公开号 26-36
德国WGK号 3

产品详细信息

详细说明 (English)
Packaging
1, 5 g in glass bottle
Application

• Reactant for preparation of bisindolyl pyrimidinones analogs of PKC inhibitor LY3335311
• Reactant for preparation of (heteroaryl)(carboxamido)arylpyrrole derivatives as Cdc7 kinase inhibitors, antitumor and antiproliferative agents2
• Reactant for preparation of (pyrrolidinylmethoxy)cyclohexanecarboxylic acids as antigen-4 (VLA-4) antagonists3
• Reactant for preparation of EphB3 receptor tyrosine kinase inhibitors4
• Reactant for preparation of pyrazolodiazepine derivatives as human P2X7 receptor antagonists5
• Reactant for preparation of potent nonpeptidic urotensin II receptor agonists6
• Reactant for preparation of pyrrolizidine esters, amides, and ureas as 5-HT4 receptor ligands7
详细说明 (简体中文)
包装
1, 5 g in glass bottle
Application

• Reactant for preparation of bisindolyl pyrimidinones analogs of PKC inhibitor LY3335311
• Reactant for preparation of (heteroaryl)(carboxamido)arylpyrrole derivatives as Cdc7 kinase inhibitors, antitumor and antiproliferative agents2
• Reactant for preparation of (pyrrolidinylmethoxy)cyclohexanecarboxylic acids as antigen-4 (VLA-4) antagonists3
• Reactant for preparation of EphB3 receptor tyrosine kinase inhibitors4
• Reactant for preparation of pyrazolodiazepine derivatives as human P2X7 receptor antagonists5
• Reactant for preparation of potent nonpeptidic urotensin II receptor agonists6
• Reactant for preparation of pyrrolizidine esters, amides, and ureas as 5-HT4 receptor ligands7

参考文献