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1-甲基吲哚-2-甲酸_分子结构_CAS_16136-58-6)
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1-甲基吲哚-2-甲酸

产品号 134155 公司名称 Sigma Aldrich
CAS号 16136-58-6 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 98% 电子邮件
保 存 Chembase数据库ID: 15623

产品价格信息

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产品别名

标题
1-Methylindole-2-carboxylic acid
IUPAC标准名
1-methyl-1H-indole-2-carboxylic acid
IUPAC传统名
1-methylindole-2-carboxylic acid
别名
NSC 68357

产品登记号

CAS号 16136-58-6
MDL号 MFCD00005801
PubChem SID 24848134

产品性质

Empirical Formula (Hill Notation) C10H9NO2
纯度 98%
熔点 212-213 °C (dec.)(lit.)
GHS危险品标识 GHS07
GHS警示词 Warning
GHS危险声明 H302-H315-H319-H335
欧盟危险性物质标志 有害性(Harmful) 有害性(Harmful) (Xn)
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 P261-P305 + P351 + P338
危险公开号 22-36/37/38
RTECS编号 NL6012400
安全公开号 26
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 keto-indoles as novel indoleamine 2,3-dioxygenase (IDO) inhibitors1
• Reactant for synthesis of fenbufen and ethacrynic acid derivatives as potential antitumor agents via amide coupling reactions2
• Reactant for diastereoselective synthesis of vinylated heterocycles via ruthenium-catalyzed oxidative vinylation with alkenes3
• Reactant for synthesis of 2,3-dihalo indoles via hypervalent iodine mediated decarboxylative halogenation4
• Reactant for preparation of α-ketoamides as cathepsin S inhibitors with potential applications against tumor invasion and angiogenesis5
• Reactant for preparation of anthranilic acid mimics as bacterial translation inhibitors6
详细说明 (简体中文)
包装
1, 5 g in glass bottle
Application

• Reactant for preparation of keto-indoles as novel indoleamine 2,3-dioxygenase (IDO) inhibitors1
• Reactant for synthesis of fenbufen and ethacrynic acid derivatives as potential antitumor agents via amide coupling reactions2
• Reactant for diastereoselective synthesis of vinylated heterocycles via ruthenium-catalyzed oxidative vinylation with alkenes3
• Reactant for synthesis of 2,3-dihalo indoles via hypervalent iodine mediated decarboxylative halogenation4
• Reactant for preparation of α-ketoamides as cathepsin S inhibitors with potential applications against tumor invasion and angiogenesis5
• Reactant for preparation of anthranilic acid mimics as bacterial translation inhibitors6

参考文献