147022-24-0

Basic information

• Product Name: (4-chlorophenyl)(naphthalene-2-yl)methanol
• Synonyms: (4-chlorophenyl)(naphthalene-2-yl)methanol
• CAS NO: 147022-24-0
• Molecular Weight: 268.743
• Mol File: 147022-24-0.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: (4-chlorophenyl)(naphthalene-2-yl)methanol(CAS DataBase Reference)
• NIST Chemistry Reference: (4-chlorophenyl)(naphthalene-2-yl)methanol(147022-24-0)
• EPA Substance Registry System: (4-chlorophenyl)(naphthalene-2-yl)methanol(147022-24-0)

Safety Data

• Hazardous Substances Data: 147022-24-0(Hazardous Substances Data)

Upstream product

• 1679-18-1 4-Chlorophenylboronic acid 
• 66-99-9 β-naphthaldehyde 
• 7495-98-9 (4-chlorophenyl)(naphthalen-2-yl)methanone 

Downstream Products

• 1613376-75-2 2-[(4-chlorophenyl)(naphthalen-2-yl)methyl]benzo[d]oxazole 
• 1613376-62-7 C₂₂H₂₁ClO₂ 
• 1613376-61-6 tert-butyl (4-chlorophenyl)(2-naphthyl)methyl carbonate 
• 147022-12-6 1-[(4-Chloro-phenyl)-naphthalen-2-yl-methyl]-1H-imidazole 
• 3042-67-9 2-(4-chlorobenzyl)naphthalene 

Relevant articles and documents

Bulky N-Heterocyclic-Carbene-Coordinated Palladium Catalysts for 1,2-Addition of Arylboron Compounds to Carbonyl Compounds

The synthesis of primary, secondary, and tertiary alcohols by the 1,2-addition of arylboronic acids or boronates to carbonyl compounds, including unactivated ketones, using novel bulky yet flexible N-heterocyclic carbene (NHC)-coordinated 2,6-di(pentan-3-yl)aniline (IPent)-based cyclometallated palladium complexes (CYPs) as catalysts is reported. The PhS-IPent-CYP-catalyzed reactions are efficient at low catalyst loadings (0.02–0.3 mol% Pd), and the exceptional catalytic activity for 1,2-addition is attributed to the steric bulk of the NHC ligand. These reactions can yield a wide range of functionalized benzylic alcohols that are difficult to synthesize by classical protocols using highly active organomagnesium or lithium reagents.

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