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吲哚-5-羧酸_分子结构_CAS_1670-81-1)
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吲哚-5-羧酸

产品号 I2250 公司名称 Sigma Aldrich
CAS号 1670-81-1 公司网站 http://www.sigmaaldrich.com
分子式 C9H7NO2 电 话 1-800-521-8956
分子量 161.15738 传 真
纯 度 ~95% (TLC) 电子邮件
保 存 Chembase数据库ID: 13652

产品价格信息

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产品别名

标题
Indole-5-carboxylic acid
IUPAC标准名
1H-indole-5-carboxylic acid
IUPAC传统名
1H-indole-5-carboxylic acid
别名
5-Carboxyindole

产品登记号

CAS号 1670-81-1
EC号 216-799-6
MDL号 MFCD00005678
Beilstein号 124391
PubChem SID 24895968

产品性质

Empirical Formula (Hill Notation) C9H7NO2
纯度 ~95% (TLC)
熔点 211-213 °C(lit.)
MSDS下载 下载链接
个人保护装置 Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
保存温度 -20°C
德国WGK号 3

产品详细信息

详细说明 (English)
Application

• Reactant for preparation of tryptophan dioxygenase inhibitors pyridyl-ethenyl-indoles, as potential anticancer immunomodulators1
• Reactant for preparation of indolyl-quinolines via metal- and solvent-free autoxidative coupling reaction2
• Reactant for preparation of anthranilic acids using bromamine-B oxidant and palladium chloride catalyst3
• Reactant for synthesis of indirubin derivatives4
• Reactant for preparation of amide conjugates with ketoprofen, as inhibitors of Gli1-mediated transcription in Hedgehog pathway5
• Reactant for preparation of piperazine-bisamide analogs as human growth hormone secretagogue receptor antagonists for treatment of obesity6
详细说明 (简体中文)
Application

• Reactant for preparation of tryptophan dioxygenase inhibitors pyridyl-ethenyl-indoles, as potential anticancer immunomodulators1
• Reactant for preparation of indolyl-quinolines via metal- and solvent-free autoxidative coupling reaction2
• Reactant for preparation of anthranilic acids using bromamine-B oxidant and palladium chloride catalyst3
• Reactant for synthesis of indirubin derivatives4
• Reactant for preparation of amide conjugates with ketoprofen, as inhibitors of Gli1-mediated transcription in Hedgehog pathway5
• Reactant for preparation of piperazine-bisamide analogs as human growth hormone secretagogue receptor antagonists for treatment of obesity6

参考文献