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Ethyl 5-methylindole-2-carboxylate_Molecular_structure_CAS_16382-15-3)
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Ethyl 5-methylindole-2-carboxylate

Catalog No. 663190 Name Sigma Aldrich
CAS Number 16382-15-3 Website http://www.sigmaaldrich.com
M. F. C12H13NO2 Telephone 1-800-521-8956
M. W. 203.23712 Fax
Purity 97% Email
Storage Chembase ID: 107178

SYNONYMS

Title
5-甲基吲哚-2-羧酸乙酯
IUPAC name
ethyl 5-methyl-1H-indole-2-carboxylate
IUPAC Traditional name
ethyl 5-methyl-1H-indole-2-carboxylate
Synonyms
5-Methylindole-2-carboxylic acid ethyl ester
NSC 30928

DATABASE IDS

MDL Number MFCD00022703
PubChem SID 24884618
CAS Number 16382-15-3

PROPERTIES

Empirical Formula (Hill Notation) C12H13NO2
Purity 97%
Melting Point 160-164 °C
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, 5 g in glass bottle
Application

• Reactant for synthesis of oxazino[4,3-a]indoles via cascade addition-cyclization reactions1
• Reactant for preparation of indolecarboxamides as cannabinoid CB1 receptor antagonists2
• Reactant for preparation of indole-3-propionic acids as antiinflammatory and analgesic agents3
• Reactant for Friedel-Crafts acylation with nitrobenzoyl chloride4
• Reactant for oximation reactions5
Description (简体中文)
包装
1, 5 g in glass bottle
Application

• Reactant for synthesis of oxazino[4,3-a]indoles via cascade addition-cyclization reactions1
• Reactant for preparation of indolecarboxamides as cannabinoid CB1 receptor antagonists2
• Reactant for preparation of indole-3-propionic acids as antiinflammatory and analgesic agents3
• Reactant for Friedel-Crafts acylation with nitrobenzoyl chloride4
• Reactant for oximation reactions5

REFERENCES