147022-23-9

Basic information

• Product Name: (4-fluorophenyl)(1-naphthyl)methanol
• Synonyms: (4-fluorophenyl)(1-naphthyl)methanol
• CAS NO: 147022-23-9
• Molecular Weight: 252.288
• Mol File: 147022-23-9.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: (4-fluorophenyl)(1-naphthyl)methanol(CAS DataBase Reference)
• NIST Chemistry Reference: (4-fluorophenyl)(1-naphthyl)methanol(147022-23-9)
• EPA Substance Registry System: (4-fluorophenyl)(1-naphthyl)methanol(147022-23-9)

Safety Data

• Hazardous Substances Data: 147022-23-9(Hazardous Substances Data)

Upstream product

• 1765-93-1 4-fluoroboronic acid 
• 66-77-3 1-naphthaldehyde 
• 448-59-9 tris(4-fluorophenyl)boroxine 
• 90-11-9 1-Bromonaphthalene 
• 459-57-4 4-fluorobenzaldehyde 
• 147022-30-8 (4-fluorophenyl)(naphthalene-4-yl)methanone 

Downstream Products

• 1365911-78-9 4-(4-(4-fluorobenzyl)naphthalen-1-yl)morpholine 
• 1333506-66-3 (E)-diethyl 2-(1-(4-fluorobenzylidene)-1,2-dihydronaphthalen-2-yl)malonate 
• 1270742-58-9 1-(chloro(4-fluorophenyl)methyl)naphthalene 
• 147022-06-8 1-[(4-Fluoro-phenyl)-naphthalen-1-yl-methyl]-1H-imidazole 

Relevant articles and documents

Palladium-catalyzed amination of chloromethylnaphthalene and chloromethylanthracene derivatives with various amines

Palladium-catalyzed amination of chloromethylnaphthalene and chloromethylanthracene derivatives to produce naphthylamines and anthrylamines in satisfactory to good yields has been developed. The unprecedented amination reactions proceeded smoothly under mild conditions in the presence of Pd(PPh3)4 as a catalyst.

Use of cheaper metal than Rh, CHCl3-free Pd catalyst, in 1,2-addition of aromatic aldehydes with arylboronic acids

Pd(OAc)2-(±)-tol-BINAP-catalyzed arylation reaction of aromatic aldehydes with arylboronic acids in the absence of CHCl3 is described.

Research on antibacterial and antifungal agents. 16. Synthesis and antifungal activities of 1-[α-(1-naphthyl)benzyl]imidazole derivatives and related 2-naphthyl isomers

Some 1-arylmethylimidazoles bearing a naphthyl group at the α position of benzyl moiety have been synthesized and tested as antifungal agents against Candida albicans and Candida spp. Such derivatives resemble bifonazole and naftifine, two important antim