916432-92-3

Basic information

• Product Name: 1-(1-benzyloxy-3-methylnaphthalen-4-yloxy)propan-2-one
• Synonyms: 1-(1-benzyloxy-3-methylnaphthalen-4-yloxy)propan-2-one
• CAS NO: 916432-92-3
• Molecular Weight: 320.388
• Mol File: 916432-92-3.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 1-(1-benzyloxy-3-methylnaphthalen-4-yloxy)propan-2-one(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(1-benzyloxy-3-methylnaphthalen-4-yloxy)propan-2-one(916432-92-3)
• EPA Substance Registry System: 1-(1-benzyloxy-3-methylnaphthalen-4-yloxy)propan-2-one(916432-92-3)

Safety Data

• Hazardous Substances Data: 916432-92-3(Hazardous Substances Data)

Upstream product

• 2211-27-0 4-acetoxy-3-methyl-1-naphthol 
• 573-20-6 menadiol di(acetate) 
• 53772-20-6 1-benzyloxy-3-methylnaphthalen-4-yl acetate 
• 78-95-5 chloroacetone 

Downstream Products

• 24615-04-1 4-Hydroxy-1-(β-propyloxy)-2-methyl-naphthalin 

Relevant articles and documents

Synthesis and cytotoxicity of 9-substituted benzo[de]chromene-7,8-dione and 5-benzyl-9-substituted benzo[de]chromene-7,8-dione

New Mansonone analogues of 9-substitued benzo[de]chromene-7,8-dione 5b-e and 5-benzyl-9-substitued benzo[de]chromene-7,8-dione 6a-e were prepared through a modified route. The first step involved a bulky base t-butylamine mediated regioselective deacetylation of 2-substituted-1,4-naphth-diyl diacetate, resulting in obtaining of monoacetate 4-acetate 2 in high yield. The mechanism of cyclization, debenzylation, and oxidation for the formation of 5a-e and 6a-e were discussed. The cytotoxicity of the prepared compounds 5 and 6 were comparable with naturally occurring Mansonone F. Copyright Taylor & Francis Group, LLC.