3588-80-5

Basic information

• Product Name: 5-Methoxy-1-naphthalenol
• Synonyms: 5-Methoxy-1-naphthalenol;5-Methoxy-1-naphthol;5-METHOXYNAPHTHALEN-1-OL
• CAS NO: 3588-80-5
• Molecular Formula: C₁₁H₁₀O₂
• Molecular Weight: 174.1959
• Product Categories: Aromatics;Miscellaneous Reagents
• Mol File: 3588-80-5.mol
• Article Data: 6

Chemical Properties

• Appearance: /
• Storage Temp.: Refrigerator
• Solubility: DMSO (Slightly), Methanol (Slightly)
• CAS DataBase Reference: 5-Methoxy-1-naphthalenol(CAS DataBase Reference)
• NIST Chemistry Reference: 5-Methoxy-1-naphthalenol(3588-80-5)
• EPA Substance Registry System: 5-Methoxy-1-naphthalenol(3588-80-5)

Safety Data

• Hazardous Substances Data: 3588-80-5(Hazardous Substances Data)

Usage

Chemical Properties

Brown Solid

Uses

5-Methoxy-1-naphthalenol (cas# 3588-80-5) is a compound useful in organic synthesis.

Upstream product

• 83-56-7 1,5-dihydroxynaphthalene 
• 77-78-1 dimethyl sulfate 
• 67-56-1 methanol 
• 10075-63-5 1,5-dimethoxynaphthalene 
• 33892-75-0 5-Methoxy-1-tetralone 
• 5123-13-7 5,5-dimethyl-2-phenyl-1,3,2-dioxaborinane 
• 64725-89-9 1-benzoyloxy-5-methoxy naphthalene 

Downstream Products

• 31461-16-2 2-(8-hydroxy-4-methoxy-[1]naphthoyl)-benzoic acid 
• 60963-09-9 1-(2,6-Dichloro-4-nitro-phenoxy)-5-methoxy-naphthalene 
• 79786-98-4 1-Hydroxy-5-methoxynaphthalin-2-carbonsaeure 
• 128462-00-0 C₃₁H₂₈O₇ 
• 128461-99-4 C₃₁H₂₈O₇ 
• 61539-67-1 5-methoxy[1,2]naphthoquinone 
• 4923-61-9 5-methoxynaphthoquinone 
• 481-39-0 5-hydroxynaphtho-1,4-quinone 
• 101303-83-7 8-Hydroxy-4-methoxy-1,2-naphthochinon 
• 37721-75-8 tetrabromo-p-cresol 
• 110387-91-2 4-nitro-5-methoxy-1-hydroxynaphthalene 
• 110387-90-1 1-hydroxy-5-methoxy-2-nitronaphthalene 
• 64725-89-9 1-benzoyloxy-5-methoxy naphthalene 
• 75716-81-3 5-methoxy-1-naphthyl cyclohexanecarboxylate 

Relevant articles and documents

Isomerization of 7-oxabenzonorbornadienes into naphthols catalyzed by [RuCl2(CO)3]2

(Chemical Equation Presented) Ruthenium-catalyzed isomerization of 7-oxanorbornadienes into naphthols was investigated. Among the various ruthenium catalysts tested, [RuCl2(CO)3]2 gave the highest yields in the isomerizati

An efficient method for demethylation of aryl methyl ethers

A new efficient method for demethylation of aryl methyl ethers using iodocyclohexane in DMF under reflux condition is described.

HALOGENATION REGIOSELECTIVE EN SERIE AROMATIQUE-II CHLORATION DES NAPHTOLS ET LEURS ETHERS A L'AIDE DE REACTIFS METTANT EN JEU DES INTERACTIONS DU TYPE DONNEUR-ACCEPTEUR

The regispecific chlorination of naphtols by hexachlorocyclohexadienones as selective chlorinating reagents is described.The selectivity attained is better than that which we have obtained with phenol derivatives and confirms the importance of the donor-acceptor interaction between the reagent and the naphthol during the chlorination.