37096-98-3

Basic information

• Product Name: 14-(3-fluorophenyl)-14H-dibenzo[a,j]xanthene
• Synonyms: 14-(3-fluorophenyl)-14H-dibenzo[a,j]xanthene
• CAS NO: 37096-98-3
• Molecular Weight: 376.43
• Mol File: 37096-98-3.mol
• Article Data: 23

Chemical Properties

• CAS DataBase Reference: 14-(3-fluorophenyl)-14H-dibenzo[a,j]xanthene(CAS DataBase Reference)
• NIST Chemistry Reference: 14-(3-fluorophenyl)-14H-dibenzo[a,j]xanthene(37096-98-3)
• EPA Substance Registry System: 14-(3-fluorophenyl)-14H-dibenzo[a,j]xanthene(37096-98-3)

Safety Data

• Hazardous Substances Data: 37096-98-3(Hazardous Substances Data)

Upstream product

• 135-19-3 β-naphthol 
• 351-24-6 1-(3-fluorobenzylidene)-2-phenylhydrazine 
• 456-48-4 3-Fluorobenzaldehyde 

Relevant articles and documents

Functionalized mesoporous materials as efficient organocatalysts for the syntheses of xanthenes

Highly efficient and recyclable heterogeneous organocatalysts containing acidic functional groups such as CO2H and SO3H have been synthesized by post-synthesis modification of 2D-hexagonal mesoporous silica materials SBA-15 and MCM-4

Br?nsted Acidic Ionic Liquid-Catalyzed Synthesis of 14-Aryl-14H-dibenzo[a,j]xanthenes with Controlled Microwave Heating under Solvent-Free Conditions

Abstract: 1-Methyl-3-sulfo-1H-imidazol-3-ium chloride([Msim]Cl) catalyzed the condensation of β-naphthol with aromatic aldehydesunder microwave irradiation. This method is efficient to synthesizedibenzoxanthene derivatives in excellent yields, and the cat

1,4-Diazaniumbicyclo[2.2.2]octane diacetate: As an effective, new and reusable media for the synthesis of 14-aryl-14H-dibenzo[a,j]xanthenes

A general synthetic route to dibenzoxanthenes has been developed using 1,4-diazaniumbicyclo[2.2.2]octane diacetate as a new bis ionic liquid under thermal and solvent free condition. This method provides several advantages such as a simple work-up, environmental friendliness and shorter reaction time along with high yields. All of the synthesized compounds were characterized by infrared spectroscopy, 1H and 13C spectroscopy and elemental analyses.