2,5-Dimethylindole

2,5-Dimethylindole
  • CAS No.:1196-79-8
Other grades of this product :
2,5-Dimethylindole Basic information
Description Sources
Product Name:2,5-Dimethylindole
Synonyms:1H-Indole, 2,5-dimethyl-;2,5-DIMETHYL-1H-INDOLE;2,5-DIMETHYLINDOLE;2,5-Dimethylindole,97%;2,5-Dimethylindole 97%;Indole, 2,5-dimethyl-;2,5-Dimethylindole&gt
CAS:1196-79-8
MF:C10H11N
MW:145.2
EINECS:214-816-1
Product Categories:Heterocycle-Indole series;Building Blocks;Heterocyclic Compounds;heterocyclic/Aliphatic series;Heterocyclic Building Blocks;Indoles;Indoles and derivatives;Indole
Mol File:1196-79-8.mol
2,5-Dimethylindole Chemical Properties
Melting point 112-113 °C (lit.)
Boiling point 254.33°C (rough estimate)
density 1.0353 (rough estimate)
refractive index 1.5000 (estimate)
storage temp. Keep in dark place,Inert atmosphere,Room temperature
solubility soluble in Methanol
form Solid
pka17.75±0.30(Predicted)
color Off-white to pale pink or light brown
CAS DataBase Reference1196-79-8(CAS DataBase Reference)
NIST Chemistry Reference1H-indole, 2,5-dimethyl-(1196-79-8)
Safety Information
Hazard Codes Xi
Risk Statements 37/38-41
Safety Statements 26-39
WGK Germany 3
Hazard Note Irritant
HS Code 29339900
MSDS Information
ProviderLanguage
2,5-Dimethylindole English
SigmaAldrich English
2,5-Dimethylindole Usage And Synthesis
Description2, 5-Dimethylindole is a kind of carbazole-system derived indole compound, which is valuable in the manufacturing of perfume. It is also a useful chemical intermediate. It is usually used as reactant in the following reaction: stereoselective synthesis of indolines via palladium-catalyzed asymmetric hydrogenation of unprotected indoles; stereoselective preparation of substituted indoles via rhodium-catalyzed enantioselective coupling reaction of indoles with diazo compounds; enantioselective synthesis of fluorene derivatives via Friedel-Crafts reactions; preparation of bis-indolyldihydroxybenzoquinones by addition indoles to dichlorobenzoquinone promoted by Bronsted acid; Reaction with hydroxypyrazolines.
Sourceshttps://www.sigmaaldrich.com/catalog/product/aldrich/d166006?lang=en&region=US https://books.google.com/books?isbn=0470188073
Chemical PropertiesOff-white to pale pink or light brown solid
Uses
  • Reactant in stereoselective preparation of substituted indoles via rhodium-catalyzed enantioselective coupling reaction of indoles with diazo compounds
  • Reactant in stereoselective synthesis of indolines via palladium-catalyzed asymmetric hydrogenation of unprotected indoles
  • Reactant in enantioselective synthesis of fluorene derivatives via Friedel-Crafts reactions
  • Reactant in preparation of bis-indolyldihydroxybenzoquinones by addition indoles to dichlorobenzoquinone promoted by Bronsted acid
  • Reactant in reaction with hydroxypyrazolines
2,5-Dimethylindole Preparation Products And Raw materials

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