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Indole-5-carboxylic acid_Molecular_structure_CAS_1670-81-1)
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Indole-5-carboxylic acid

Catalog No. I5400 Name Sigma Aldrich
CAS Number 1670-81-1 Website http://www.sigmaaldrich.com
M. F. C9H7NO2 Telephone 1-800-521-8956
M. W. 161.15738 Fax
Purity 99% Email
Storage Chembase ID: 13652

SYNONYMS

Title
吲哚-5-羧酸
IUPAC name
1H-indole-5-carboxylic acid
IUPAC Traditional name
1H-indole-5-carboxylic acid
Synonyms
5-Carboxyindole

DATABASE IDS

CAS Number 1670-81-1
EC Number 216-799-6
MDL Number MFCD00005678
Beilstein Number 124391
PubChem SID 24896068

PROPERTIES

Empirical Formula (Hill Notation) C9H7NO2
Purity 99%
Melting Point 211-213 °C(lit.)
MSDS Link Download
Personal Protective Equipment Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
German water hazard class 3

DETAILS

Description (English)
Packaging
1 g in glass bottle
5 g in poly bottle
Application

• Reactant for preparation of tryptophan dioxygenase inhibitors pyridyl-ethenyl-indoles, as potential anticancer immunomodulators1
• Reactant for preparation of indolyl-quinolines via metal- and solvent-free autoxidative coupling reaction2
• Reactant for preparation of anthranilic acids using bromamine-B oxidant and palladium chloride catalyst3
• Reactant for synthesis of indirubin derivatives4
• Reactant for preparation of amide conjugates with ketoprofen, as inhibitors of Gli1-mediated transcription in Hedgehog pathway5
• Reactant for preparation of piperazine-bisamide analogs as human growth hormone secretagogue receptor antagonists for treatment of obesity6
Description (简体中文)
包装
1 g in glass bottle
5 g in poly bottle
Application

• Reactant for preparation of tryptophan dioxygenase inhibitors pyridyl-ethenyl-indoles, as potential anticancer immunomodulators1
• Reactant for preparation of indolyl-quinolines via metal- and solvent-free autoxidative coupling reaction2
• Reactant for preparation of anthranilic acids using bromamine-B oxidant and palladium chloride catalyst3
• Reactant for synthesis of indirubin derivatives4
• Reactant for preparation of amide conjugates with ketoprofen, as inhibitors of Gli1-mediated transcription in Hedgehog pathway5
• Reactant for preparation of piperazine-bisamide analogs as human growth hormone secretagogue receptor antagonists for treatment of obesity6

REFERENCES