64725-89-9

Basic information

• Product Name: 1-Naphthalenol, 5-methoxy-, benzoate
• CAS NO: 64725-89-9
• Molecular Formula: C18H14O3
• Molecular Weight: 278.307
• Mol File: 64725-89-9.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 1-Naphthalenol, 5-methoxy-, benzoate(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Naphthalenol, 5-methoxy-, benzoate(64725-89-9)
• EPA Substance Registry System: 1-Naphthalenol, 5-methoxy-, benzoate(64725-89-9)

Safety Data

• Hazardous Substances Data: 64725-89-9(Hazardous Substances Data)

Upstream product

• 3588-80-5 5-methoxynaphthalen-1-ol 
• 98-88-4 benzoyl chloride 

Downstream Products

• 3588-80-5 5-methoxynaphthalen-1-ol 
• 75716-80-2 1-hydroxy-5-methoxy-2-naphthyl phenyl ketone 
• 78378-33-3 4-methoxy-8-benzoyloxynaphthophenone 
• 78378-29-7 4-methoxy-8-benzoyloxypropionaphthone 
• 70340-74-8 4-methoxy-8-hydroxy-1-naphthyl benzyl ketone 
• 78378-30-0 4-methoxy-8-benzoyloxynaphthyl benzyl ketone 
• 80032-52-6 Benzoic acid 5-methoxy-8-[(E)-3-(4-methoxy-phenyl)-acryloyl]-naphthalen-1-yl ester 
• 78378-31-1 4-methoxy-8-benzoyloxy-1-naphthaldehyde 
• 73512-28-4 1-cinnamoyl-4-methoxy-8-hydroxynaphthalene 
• 80032-53-7 8-benzoyloxy-4-methoxy-1-naphthyl 1,2-dibromo-2-phenylethyl ketone 
• 80032-54-8 Benzoic acid 8-[2,3-dibromo-3-(4-methoxy-phenyl)-propionyl]-5-methoxy-naphthalen-1-yl ester 
• 75716-78-8 3-hydroxy-5-methoxy-1,4-dioxo-1,4-dihydro-2-naphthyl cyclohexyl ketone 
• 75731-74-7 5-methoxy-1,4-dioxo-1,4-dihydro-2-naphthyl cyclohexyl ketone 
• 75716-79-9 1-hydroxy-5-methoxy-2-naphthyl cyclohexyl ketone 

Relevant articles and documents

PHOTO FRIES REARRANGEMENTS OF 1-NAPHTHYL ESTERS IN THE SYNTHESIS OF 2-ACYLNAPHTHOQUINONES

The photo Fries rearrangements of esters of 1-naphthol and 5-methoxy-1-naphthol to the corresponding 1-hydroxy-2-acylnaphthalenes have been carried out.The best yield (70percent) was obtained by irradiating 5-methoxy-1-naphthyl acetate in ethyl acetate.By contrast the yield from 1-naphthyl acetate under similar conditions was 40percent.Oxidation of 1-hydroxy-5-methoxy-2-naphthyl cyclohexyl ketone with thallium trinitrate gave the corresponding 1,4-quinone.These results provide a method for the regioselective synthesis of tricyclic analogues of adriamycinone.