1041143-98-9

Basic information

• Product Name: 3,6-Difluorocarbazole
• Synonyms: 3,6-Difluoro-9H-carbazole;3,6-Difluorocarbazole
• CAS NO: 1041143-98-9
• Molecular Formula: C12H7F2N
• Molecular Weight: 203.1874864
• Mol File: 1041143-98-9.mol
• Article Data: 9

Chemical Properties

• Melting Point: 198.9-200.8 °C
• Boiling Point: 362.5±22.0 °C(Predicted)
• Appearance: /
• Density: 1.407±0.06 g/cm3(Predicted)
• PKA: 15.96±0.30(Predicted)
• CAS DataBase Reference: 3,6-Difluorocarbazole(CAS DataBase Reference)
• NIST Chemistry Reference: 3,6-Difluorocarbazole(1041143-98-9)
• EPA Substance Registry System: 3,6-Difluorocarbazole(1041143-98-9)

Safety Data

• Hazardous Substances Data: 1041143-98-9(Hazardous Substances Data)

Upstream product

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• 1003-98-1 2-bromo-4-fluoroaniline 
• 2106-02-7 2-chloro-4-fluoroaniline 
• 460-00-4 1-Bromo-4-fluorobenzene 
• 1041143-87-6 (2-chloro-4-fluorophenyl)(4-fluorophenyl)amine 

Relevant articles and documents

COMPOUND FOR ORGANIC OPTOELECTRONIC DEVICE, COMPOSITION FOR ORGANIC OPTOELECTRONIC DEVICE AND ORGANIC OPTOELECTRONIC DEVICE AND DISPLAY DEVICE

The present specification relates to a compound for an organic optoelectronic device represented by chemical formula 1, a composition for an organic optoelectronic device including the same, an organic optoelectronic device, and a display device. Details

Fluorine-substituted bimolecular carbazole derivative as well as preparation method and application thereof

The invention discloses a fluorine-substituted bimolecular carbazole derivative represented by a formula (I) or pharmaceutically acceptable salt thereof. R1, R2, R3, R4 and R5 are defined in the specification. The fluorine-substituted bimolecular carbazole derivative or the pharmaceutically acceptable salt thereof provided by the invention can be used for preparing a DNA methyltransferase inhibitor or a histone demethylase inhibitor, and in-vitro cancer cell anti-proliferation tests prove that the fluorine-substituted bimolecular carbazole derivative has anti-proliferation activity on cancer cells.

Carbazole-containing amides and ureas: Discovery of cryptochrome modulators as antihyperglycemic agents

A series of novel carbazole-containing amides and ureas were synthesized. A structure–activity relationship study of these compounds led to the identification of potent cryptochrome modulators. Based on the desired pharmacokinetic/pharmacodynamic parameters and the results of efficacy studies in db/db mice, compound 50 was selected for further profiling.