2,5-Dimethylindole 1196-79-8 CAS NO.1196-79-8
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- Min.Order: 1 Kilogram
- Payment Terms: L/C,T/T
- Available Specifications:
A(10-150)Kilogram
- Product Details
Keywords
- 2,5-Dimethylindole 1196-79-8
- 2,5-Dimethylindole 1196-79-8
- 2,5-Dimethylindole 1196-79-8
Quick Details
- ProName: 2,5-Dimethylindole 1196-79-8
- CasNo: 1196-79-8
- Molecular Formula: C10H11N
- Appearance: Solid
- Application: Organic Chemicals
- DeliveryTime: according to client's demand quantity
- PackAge: as requested
- Port: SHANGHAI
- ProductionCapacity: 100 Metric Ton/Year
- Purity: 99%
- Storage: room temperature
- Transportation: by Sea
- LimitNum: 1 Kilogram
- Heavy metal: 0.01
- Grade: Industrial Grade,Pharma Grade
- Transportation: LCL
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