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5-Methoxy-3-indoleacetic acid_Molecular_structure_CAS_3471-31-6)
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5-Methoxy-3-indoleacetic acid

Catalog No. M14935 Name Sigma Aldrich
CAS Number 3471-31-6 Website http://www.sigmaaldrich.com
M. F. C11H11NO3 Telephone 1-800-521-8956
M. W. 205.20994 Fax
Purity 98% Email
Storage Chembase ID: 68737

SYNONYMS

Title
5-甲氧基-3-吲哚乙酸
IUPAC name
2-(5-methoxy-1H-indol-3-yl)acetic acid
IUPAC Traditional name
5-methoxyindole-3-acetic acid
Synonyms
2-(5-Methoxy-3-indolyl)acetic acid

DATABASE IDS

CAS Number 3471-31-6
PubChem SID 24896651
EC Number 222-438-3
Beilstein Number 187161
MDL Number MFCD00005638

PROPERTIES

Empirical Formula (Hill Notation) C11H11NO3
Purity 98%
Melting Point 145-148 °C (dec.)(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
Application

• Reactant for preparation of aryloxybenzothiazoles as inhibitors of NO production1
• Reactant for preparation of transcription inhibitors of novel Gli1 as antitumor agents
• Reactant for preparation of indole derivatives as NR2B/NMDA receptor antagonists2
• Reactant for preparation of indolyl esters and amides related to indomethacin as selective COX-2 inhibitors3
• Reactant for preparation of quinoline salicylic acid series of P-selectin antagonists4
• Reactant for preparation of prostaglandin D2 receptor antagonists5
Description (简体中文)
包装
1 g in glass bottle
Application

• Reactant for preparation of aryloxybenzothiazoles as inhibitors of NO production1
• Reactant for preparation of transcription inhibitors of novel Gli1 as antitumor agents
• Reactant for preparation of indole derivatives as NR2B/NMDA receptor antagonists2
• Reactant for preparation of indolyl esters and amides related to indomethacin as selective COX-2 inhibitors3
• Reactant for preparation of quinoline salicylic acid series of P-selectin antagonists4
• Reactant for preparation of prostaglandin D2 receptor antagonists5

REFERENCES