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Indole-2-carboxylic acid_Molecular_structure_CAS_1477-50-5)
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Indole-2-carboxylic acid

Catalog No. 57220 Name Sigma Aldrich
CAS Number 1477-50-5 Website http://www.sigmaaldrich.com
M. F. C9H7NO2 Telephone 1-800-521-8956
M. W. 161.15738 Fax
Purity ≥98.0% (T) Email
Storage Chembase ID: 13653

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
MSDS Link Download
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

REFERENCES