51640-60-9

Basic information

• Product Name: 1,5-dimethyl-9H-carbazole
• Synonyms: 1,5-Dimethyl-9H-carbazole; Carbazole, 1,5-dimethyl-
• CAS NO: 51640-60-9
• Molecular Formula: C₁₄H₁₃N
• Molecular Weight: 195.2597
• Mol File: 51640-60-9.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 383°C at 760 mmHg
• Flash Point: 170.8°C
• Density: 1.158g/cm³
• Vapor Pressure: 9.99E-06mmHg at 25°C
• Refractive Index: 1.712
• CAS DataBase Reference: 1,5-dimethyl-9H-carbazole(CAS DataBase Reference)
• NIST Chemistry Reference: 1,5-dimethyl-9H-carbazole(51640-60-9)
• EPA Substance Registry System: 1,5-dimethyl-9H-carbazole(51640-60-9)

Safety Data

• Hazardous Substances Data: 51640-60-9(Hazardous Substances Data)

Usage

Family

Carbazole family

Type

Heterocyclic aromatic compound

Characteristic feature

Presence of two methyl groups attached to the carbazole ring

Applications

a. Production of dyes and pigments
b. Organic light-emitting diodes (OLEDs)
c. Semiconductor devices

Potential properties

a. Anticancer properties
b. Antiparasitic properties

Additional use

Organic solar cells

Upstream product

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Relevant articles and documents

Reactions of arynes with nitrosoarenes - An approach to substituted carbazoles

No transition metals are necessary in the reaction of in situ generated arynes with nitrosoarenes to give substituted carbazoles. Depending on the fluoride source and the solvent, either N-arylated carbazoles or NH-carbazoles are obtained (see scheme; DME=dimethoxyethane, OTf=trifluoromethanesulfonate). In these cascades a C-C and one or two C-N bonds are formed. The reactions are easy to conduct and proceed under mild conditions. Copyright

The Chemistry of Carbazoles. VII. Syntheses of Methylcarbazoles

Thirty-six methylcarbazoles were prepared, and their synthetic methods were critically described.