76939-81-6

Basic information

• Product Name: Naphthalene, 2-bromo-1-(phenylmethoxy)-
• CAS NO: 76939-81-6
• Molecular Formula: C17H13BrO
• Molecular Weight: 313.194
• Mol File: 76939-81-6.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Naphthalene, 2-bromo-1-(phenylmethoxy)-(CAS DataBase Reference)
• NIST Chemistry Reference: Naphthalene, 2-bromo-1-(phenylmethoxy)-(76939-81-6)
• EPA Substance Registry System: Naphthalene, 2-bromo-1-(phenylmethoxy)-(76939-81-6)

Safety Data

• Hazardous Substances Data: 76939-81-6(Hazardous Substances Data)

Upstream product

• 771-15-3 2-bromo-1-naphthol 
• 100-44-7 benzyl chloride 
• 90-15-3 α-naphthol 
• 879-15-2 2-diazo-1,2-naphthoquinone 
• 100-39-0 benzyl bromide 
• 2050-49-9 2,4-dibromo-1-naphthol 

Downstream Products

• 138123-06-5 1-(4-Benzyloxy-naphthalen-2-yl)-ethanone 

Relevant articles and documents

Rh(II)-Catalyzed Synthetic Strategy for Diverse and Functionalized Halonaphthalenyl Ethers and Esters from Diazo Compounds and Its Application to Polyaromatic Compounds

An efficient and simple synthesis of various functionalized halonaphthalenyl ethers and esters in moderate to good yield was achieved via rhodium(II)-catalyzed reaction of readily available diazo compounds with benzyl halides or acid halides. This methodology has several advantages, such as ease of handling, mild reaction conditions, bromine- or chlorine-free route, and the use of an effective catalyst. The synthesized compounds were further converted into valuable polyaromatic compounds using the Suzuki reaction.

The synthesis and biological activity of two analogs of the anti-HIV alkaloid michellamine B

Two simplified analogs of the dimeric naphthalenyltetrahydroisoquinoline alkaloid michellamine B [4',4''-didesmethoxy-2',2''-didesmethylmichellamine B and 6,8-dihydroxy-5-(1',1''-dihydroxy-2',2''-binaphthalen-4'-yl)-1R,3R-dim ethyl-1,2,3,4-tetrahydroisoqu