150712-57-5

Basic information

• Product Name: 6-Hydroxy-2-methoxynaphthalene
• Synonyms: 6-Hydroxy-2-methoxynaphthalene
• CAS NO: 150712-57-5
• Molecular Formula: C₁₁H₁₀O₂
• Molecular Weight: 174.1959
• Mol File: 150712-57-5.mol
• Article Data: 5

Chemical Properties

• Melting Point: 62 °C
• Boiling Point: 185-186 °C(Press: 8 Torr)
• Appearance: /
• Density: 1.193±0.06 g/cm3(Predicted)
• PKA: 9.43±0.40(Predicted)
• CAS DataBase Reference: 6-Hydroxy-2-methoxynaphthalene(CAS DataBase Reference)
• NIST Chemistry Reference: 6-Hydroxy-2-methoxynaphthalene(150712-57-5)
• EPA Substance Registry System: 6-Hydroxy-2-methoxynaphthalene(150712-57-5)

Safety Data

• Hazardous Substances Data: 150712-57-5(Hazardous Substances Data)

Upstream product

• 575-44-0 1,6-dihydroxynaphthalene 
• 67-56-1 methanol 
• 3900-49-0 1,6-dimethoxynaphthalene 
• 3470-50-6 6-Hydroxy-1-tetralone 
• 53473-35-1 5-oxo-5,6,7,8-tetrahydronaphthalen-2-yl acetate 
• 32940-15-1 5-methoxy-2-tetralone 

Downstream Products

• 105467-67-2 4-hydroxydibenzacridine 
• 1552321-21-7 C₂₈H₂₇N₃O₅S 
• 1552320-92-9 2-[4-[[2-(5-methoxy-2-naphthyl)-5,5-dioxo-7,8-dihydro-6H-thiopyrano[3,2-d]pyrimidin-4-yl]amino]phenyl]acetic acid 

Relevant articles and documents

Synthesis of β-nitro ketones from geminal bromonitroalkanes and silyl enol ethers by visible light photoredox catalysis

Various β-nitro ketones, including those bearing a β-tertiary carbon, were prepared from geminal bromonitroalkanes and trimethylsilyl enol ethers of a broad range of ketones by visible light photoredox catalysis, which were then easily converted into β-amino ketones, 1,3-amino alcohols, α,β-unsaturated ketones, β-cyano ketones and γ-nitro ketones.

Deleterious effect of 7-methyl group on glycosylation of 2-naphthols

C-Glycosylations of several 2-naphthols with different glycosyl donors have been investigated in the pursuit of the total synthesis of mayamycin (1). While glycosylations of the parent 2-naphthol are readily achievable, those of 5-methoxy-7-methyl-2-napht

Regioselective Monomethylation of Unsymmetrical Naphthalenediols with Methanolic HCl

Treatment of naphthalene-1,3-diol and naphthalene-1,7-diol with methanol containing dry hydrogen chloride at room temperature gives exclusively 3-methoxy-1-naphthol and 7-methoxy-1-naphthol, respectively.Of the other two unsymmetrical naphthalenediols, the 1,2-isomer was unreactive and the 1,6-isomer gave a mixture of regioisomers under the same conditions.Two symmetrical diols (the 1,5- and 2,7-isomers) examined by the same procedure gave the monomethyl ethers in 60-70percent yields.