Indole-2-carboxylic acid

• Catalog No.: I5109
• CAS Number: 1477-50-5
• M. F.: C9H7NO2
• M. W.: 161.15738
• Purity: 98%

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
• PubChem SID: 24895981
• CAS Number: 1477-50-5
• MDL Number: MFCD00005611

PROPERTIES

• Empirical Formula (Hill Notation): C9H7NO2
• Purity: 98%
• Gene Information: human ... SRD5A1(6715)rat ... Grin2a(24409)
• Melting Point: 202-206 °C(lit.)
• Personal Protective Equipment: Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
• German water hazard class: 3

DETAILS

Description (English)

Packaging
10, 50 g in poly bottle
5 g in glass bottle
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)

包装
10, 50 g in poly bottle
5 g in glass bottle
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