Indole-2-carboxylic acid

• Catalog No.: 57220
• CAS Number: 1477-50-5
• M. F.: C9H7NO2
• M. W.: 161.15738
• Purity: ≥98.0% (T)

SYNONYMS

• Title: 吲哚-2-羧酸
• IUPAC name: 1H-indole-2-carboxylic acid
• IUPAC Traditional name: indole-2-carboxylic acid
• Synonyms: 2-Carboxyindole; 2-羧基吲哚; NSC 16598; 2-Indolylformic acid

DATABASE IDS

• EC Number: 216-030-4
• Beilstein Number: 124132
• CAS Number: 1477-50-5
• MDL Number: MFCD00005611

PROPERTIES

• German water hazard class: 3
• Personal Protective Equipment: Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
• Empirical Formula (Hill Notation): C9H7NO2
• Grade: purum
• Ignition Residue: ≤0.05%
• Purity: ≥98.0% (T)
• Melting Point: 202-206 °C(lit.)
• Melting Point: 204-209 °C

DETAILS

Description (English)

Application

• Reactant for total synthesis of (±)-dibromophakellin and analogs1
• Reactant for synthesis of the pyrrolizidine alkaloid (±)-trachelanthamidine2
• Reactant for stereoselective preparation of renieramycin G analogs3
• Reactant for preparation of spirooxoindolepyrrolidines via reduction of indole-2-carboxylic acid followed by oxidation, condensation, reduction, amidation and Kharasch radical cyclization4
• Reactant for Pd-catalyzed cyclization5
• Reactant for preparation of N,N′-(pentane)diylbis[indolecarboxamide] and N,N′-[phenylenebis(methylene)]bis[indolecarboxamide] derivatives6

Description (简体中文)

Application

• Reactant for total synthesis of (±)-dibromophakellin and analogs1
• Reactant for synthesis of the pyrrolizidine alkaloid (±)-trachelanthamidine2
• Reactant for stereoselective preparation of renieramycin G analogs3
• Reactant for preparation of spirooxoindolepyrrolidines via reduction of indole-2-carboxylic acid followed by oxidation, condensation, reduction, amidation and Kharasch radical cyclization4
• Reactant for Pd-catalyzed cyclization5
• Reactant for preparation of N,N′-(pentane)diylbis[indolecarboxamide] and N,N′-[phenylenebis(methylene)]bis[indolecarboxamide] derivatives6