Indole-4-carboxylic acid

• Catalog No.: 246263
• CAS Number: 2124-55-2
• M. F.: C9H7NO2
• M. W.: 161.15738
• Purity: 98%

SYNONYMS

• Title: 吲哚-4-羧酸
• IUPAC name: 1H-indole-4-carboxylic acid
• IUPAC Traditional name: 1H-indole-4-carboxylic acid
• Synonyms: 4-Carboxyindole

DATABASE IDS

• PubChem SID: 24854799
• CAS Number: 2124-55-2
• MDL Number: MFCD00009739

PROPERTIES

• Empirical Formula (Hill Notation): C9H7NO2
• Purity: 98%
• Melting Point: 213-214 °C(lit.)
• GHS Signal Word: Warning
• GHS Hazard statements: H315-H319-H335
• European Hazard Symbols: Irritant (Xi)
• Personal Protective Equipment: dust mask type N95 (US), Eyeshields, Gloves
• GHS Precautionary statements: P261-P305 + P351 + P338
• Risk Statements: 36/37/38
• Safety Statements: 26-36
• German water hazard class: 3

DETAILS

Description (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

Description (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