2,5-Dimethylindole ...

2,5-Dimethylindole 1196-79-8
2,5-Dimethylindole 1196-79-8
2,5-Dimethylindole 1196-79-8
2,5-Dimethylindole 1196-79-8
2,5-Dimethylindole 1196-79-8

2,5-Dimethylindole 1196-79-8

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1 Kilogram

FOB Price: USD 230.0000

  • Min.Order :1 Kilogram
  • Purity: 99%
  • Payment Terms : L/C,T/T

Keywords

2,5-Dimethylindole 1196-79-8 2,5-Dimethylindole 1196-79-8 2,5-Dimethylindole 1196-79-8

Quick Details

  • Appearance:Solid
  • Application:Organic Chemicals
  • PackAge:as requested
  • ProductionCapacity:100|Metric Ton|Year
  • Storage:room temperature
  • Transportation:by Sea

Superiority:

Product Name: 2,5-Dimethylindole
Synonyms: 2,5-DIMETHYL-1H-INDOLE;2,5-DIMETHYLINDOLE;2,5-Dimethylindole,97%;2,5-Dimethylindole 97%;Indole, 2,5-dimethyl-;1H-Indole, 2,5-dimethyl-
CAS: 1196-79-8
MF: C10H11N
MW: 145.2
EINECS: 214-816-1
Product Categories: Indoles and derivatives;Indole;Heterocyclic Compounds;heterocyclic/Aliphatic series;Building Blocks;Heterocyclic Building Blocks;Indoles;Heterocycle-Indole series
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)
form  Solid
pka 17.75±0.30(Predicted)
color  Off-white to pale pink or light brown
CAS DataBase Reference 1196-79-8(CAS DataBase Reference)
NIST Chemistry Reference 1H-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

2,5-Dimethylindole Usage And Synthesis
Description 2, 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.

Chemical Properties Off-white to pale pink or light brown solid

Details:

Product Name: 2,5-Dimethylindole
Synonyms: 2,5-DIMETHYL-1H-INDOLE;2,5-DIMETHYLINDOLE;2,5-Dimethylindole,97%;2,5-Dimethylindole 97%;Indole, 2,5-dimethyl-;1H-Indole, 2,5-dimethyl-
CAS: 1196-79-8
MF: C10H11N
MW: 145.2
EINECS: 214-816-1
Product Categories: Indoles and derivatives;Indole;Heterocyclic Compounds;heterocyclic/Aliphatic series;Building Blocks;Heterocyclic Building Blocks;Indoles;Heterocycle-Indole series
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)
form  Solid
pka 17.75±0.30(Predicted)
color  Off-white to pale pink or light brown
CAS DataBase Reference 1196-79-8(CAS DataBase Reference)
NIST Chemistry Reference 1H-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

2,5-Dimethylindole Usage And Synthesis
Description 2, 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.

Chemical Properties Off-white to pale pink or light brown solid

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