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2,5-Dimethylindole_Molecular_structure_CAS_1196-79-8)
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2,5-Dimethylindole

Catalog No. D166006 Name Sigma Aldrich
CAS Number 1196-79-8 Website http://www.sigmaaldrich.com
M. F. C10H11N Telephone 1-800-521-8956
M. W. 145.20104 Fax
Purity 97% Email
Storage Chembase ID: 10104

SYNONYMS

Title
2,5-二甲基吲哚
IUPAC name
2,5-dimethyl-1H-indole
IUPAC Traditional name
1H-indole, 2,5-dimethyl-

DATABASE IDS

MDL Number MFCD00005621
EC Number 214-816-1
CAS Number 1196-79-8
PubChem SID 24893509

PROPERTIES

Empirical Formula (Hill Notation) C10H11N
Purity 97%
Melting Point 112-113 °C(lit.)
GHS Pictograms GHS05
GHS Pictograms GHS07
GHS Signal Word Danger
GHS Hazard statements H315-H318-H335
European Hazard Symbols Irritant Irritant (Xi)
MSDS Link Download
GHS Precautionary statements P261-P280-P305 + P351 + P338
Risk Statements 37/38-41
Safety Statements 26-39
German water hazard class 3

DETAILS

Description (English)
Packaging
1 g in glass bottle
Application

• Reactant in stereoselective preparation of substituted indoles via rhodium-catalyzed enantioselective coupling reaction of indoles with diazo compounds1
• Reactant in stereoselective synthesis of indolines via palladium-catalyzed asymmetric hydrogenation of unprotected indoles2
• Reactant in enantioselective synthesis of fluorene derivatives via Friedel-Crafts reactions3
• Reactant in preparation of bis-indolyldihydroxybenzoquinones by addition indoles to dichlorobenzoquinone promoted by Bronsted acid4
• Reactant in reaction with hydroxypyrazolines5
Description (简体中文)
包装
1 g in glass bottle
Application

• Reactant in stereoselective preparation of substituted indoles via rhodium-catalyzed enantioselective coupling reaction of indoles with diazo compounds1
• Reactant in stereoselective synthesis of indolines via palladium-catalyzed asymmetric hydrogenation of unprotected indoles2
• Reactant in enantioselective synthesis of fluorene derivatives via Friedel-Crafts reactions3
• Reactant in preparation of bis-indolyldihydroxybenzoquinones by addition indoles to dichlorobenzoquinone promoted by Bronsted acid4
• Reactant in reaction with hydroxypyrazolines5

REFERENCES