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5-羟基吲哚-2-甲酸_分子结构_CAS_21598-06-1)
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5-羟基吲哚-2-甲酸

产品号 55355 公司名称 Sigma Aldrich
CAS号 21598-06-1 公司网站 http://www.sigmaaldrich.com
分子式 C9H7NO3 电 话 1-800-521-8956
分子量 177.15678 传 真
纯 度 ≥97.0% (T) 电子邮件
保 存 Chembase数据库ID: 103312

产品价格信息

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产品别名

标题
5-Hydroxyindole-2-carboxylic acid
IUPAC标准名
5-hydroxy-1H-indole-2-carboxylic acid
IUPAC传统名
5-hydroxy-1H-indole-2-carboxylic acid
别名
NSC 117338

产品登记号

PubChem SID 24879337
EC号 244-468-6
Beilstein号 153214
MDL号 MFCD00005615
CAS号 21598-06-1

产品性质

Empirical Formula (Hill Notation) C9H7NO3
级别 purum
纯度 ≥97.0% (T)
熔点 249 °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)
Application

• Reactant for preparation of indole C5-O-substituted seco-cyclopropylindole analogs as potential anticancer agents
• Reactant for microwave combinatorial synthesis of indolic arylpiperazine derivatives as ligands for 5-HT1A, 5-HT2A, and 5-HT2C receptors1
• Reactant for preparation of melanins as novel nature-inspired radioprotectors2
• Reactant for preparation of 5-Hydroxyindole-2-carboxylic acid amides as histamine-3 receptor inverse agonists for the treatment of obesity3
• Reactant for preparation of conformationally constrained peptidomimetic inhibitors of signal transducer and activator of transcription 3 (Stat3)4
• Reactant for preparation of oxadiazole analogs as nonpeptidic SH2 inhibitors of tyrosine kinase ZAP-705
详细说明 (简体中文)
Application

• Reactant for preparation of indole C5-O-substituted seco-cyclopropylindole analogs as potential anticancer agents
• Reactant for microwave combinatorial synthesis of indolic arylpiperazine derivatives as ligands for 5-HT1A, 5-HT2A, and 5-HT2C receptors1
• Reactant for preparation of melanins as novel nature-inspired radioprotectors2
• Reactant for preparation of 5-Hydroxyindole-2-carboxylic acid amides as histamine-3 receptor inverse agonists for the treatment of obesity3
• Reactant for preparation of conformationally constrained peptidomimetic inhibitors of signal transducer and activator of transcription 3 (Stat3)4
• Reactant for preparation of oxadiazole analogs as nonpeptidic SH2 inhibitors of tyrosine kinase ZAP-705

参考文献