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吲哚-4-羧酸_分子结构_CAS_2124-55-2)
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吲哚-4-羧酸

产品号 246263 公司名称 Sigma Aldrich
CAS号 2124-55-2 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 98% 电子邮件
保 存 Chembase数据库ID: 15060

产品价格信息

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产品别名

标题
Indole-4-carboxylic acid
IUPAC标准名
1H-indole-4-carboxylic acid
IUPAC传统名
1H-indole-4-carboxylic acid
别名
4-Carboxyindole

产品登记号

PubChem SID 24854799
CAS号 2124-55-2
MDL号 MFCD00009739

产品性质

Empirical Formula (Hill Notation) C9H7NO2
纯度 98%
熔点 213-214 °C(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
tert-butyl esters of indole and pyrrolecarboylic acids are readily prepared by direct treatment with N,N-dimethylformamide di-tert-butyl acetal (Cat. No. 395005).8

• Reactant for preparation of substituted indole derivatives as histamine H3 antagonists1
• Reactant for preparation of potent and selective inhibitors of human reticulocyte 15-lipoxygenase-12
• Reactant for preparation of inhibitors of Gli1-mediated transcription in Hedgehog pathway3
• Reactant for preparation of pyridinyl carboxylates as SARS-CoV 3CL proinhibitors4
• Reactant for preparation of substituted bipiperidinylmethyl amides as CCR3 membrane binding ligands5
• Reactant for preparation of indole amide hydroxamic acids as potent inhibitors of histone deacetylases6
• Reactant for preparation of 2-[[[4′-chloro-[1,1-biphenyl]-4-yl]thio]methyl]-N-hydroxybutanamide derivatives as specific metalloproteinase7
Packaging
500 mg in glass bottle
详细说明 (简体中文)
Application
吡咯羧酸和吲哚的叔丁酯可以很容易的通过直接处理N,N-二甲基甲酰胺二叔丁基乙缩醛(产品目录号 395005)来制备。8

• Reactant for preparation of substituted indole derivatives as histamine H3 antagonists1
• Reactant for preparation of potent and selective inhibitors of human reticulocyte 15-lipoxygenase-12
• Reactant for preparation of inhibitors of Gli1-mediated transcription in Hedgehog pathway3
• Reactant for preparation of pyridinyl carboxylates as SARS-CoV 3CL proinhibitors4
• Reactant for preparation of substituted bipiperidinylmethyl amides as CCR3 membrane binding ligands5
• Reactant for preparation of indole amide hydroxamic acids as potent inhibitors of histone deacetylases6
• Reactant for preparation of 2-[[[4′-chloro-[1,1-biphenyl]-4-yl]thio]methyl]-N-hydroxybutanamide derivatives as specific metalloproteinase7
包装
500 mg in glass bottle

参考文献