66596-06-3

Basic information

• Product Name: 14-(3-trifluoromethylphenyl)-14-H-dibenzo[a,j]xanthene
• Synonyms: 14-(3-trifluoromethylphenyl)-14-H-dibenzo[a,j]xanthene
• CAS NO: 66596-06-3
• Molecular Weight: 426.438
• Mol File: 66596-06-3.mol

Chemical Properties

• CAS DataBase Reference: 14-(3-trifluoromethylphenyl)-14-H-dibenzo[a,j]xanthene(CAS DataBase Reference)
• NIST Chemistry Reference: 14-(3-trifluoromethylphenyl)-14-H-dibenzo[a,j]xanthene(66596-06-3)
• EPA Substance Registry System: 14-(3-trifluoromethylphenyl)-14-H-dibenzo[a,j]xanthene(66596-06-3)

Safety Data

• Hazardous Substances Data: 66596-06-3(Hazardous Substances Data)

Upstream product

• 454-89-7 3-Trifluoromethylbenzaldehyde 
• 135-19-3 β-naphthol 

Relevant articles and documents

Heterogeneous catalyst: Amberlyst-15 catalyzes the synthesis of 14-substituted-14H-dibenzo[a,j]xanthenes under solvent-free conditions

A one-pot condensation of β-naphthol with aldehydes in the presence of Amberlyst-15 to give 14-substituted-14H-dibenzo[a,j]xanthenes under solvent-free condition is described.

Camphor-10-sulfonic acid catalyzed condensation of 2-naphthol with aromatic/aliphatic aldehydes to 14-aryl/alkyl-14H-dibenzo[a,j]xanthenes

The (±)-camphor-10-sulfonic acid (CSA) catalyzed condensation of 2-naphthol with both aliphatic/aromatic aldehydes at 80 °C yielded 14-alkyl/ /aryldibenzoxanthenes as the sole products in high yields. However, the same condensation with benzaldehyde at 25

Diversity oriented synthesis of benzoxanthene and benzochromene libraries via one-pot, three-component reactions and their anti-proliferative activity

Libraries of benzoxanthenes, as well as of benzochromenes, were efficiently synthesized via one-pot, three-component reactions of 2-naphthol, aldehydes, and cyclic 1,3-diketones/malononitrile/ethyl cyanoacetate in the presence of catalytic amount of eerie

Perchloric acid-silica (HClO4·SiO2)-catalyzed synthesis of 14-alkyl- or 14-aryl-14H-dibenzo[a,,j]xanthenes and N-[(2-hydroxynaphthalen-1-yl)methyl]amides

The synthesis of 14-aryl- or 14-alkyl-14H-dibenzo[a,j]xanthenes 3 involving the treatment of naphthalen-2-ol (1) with arenecarboxaldehydes or alkanals 2 in the presence of HClO4·SiO2 as a heterogeneous catalyst was achieved (Table 1)