39110-92-4

Basic information

• Product Name: 3-METHOXY-2-NAPHTHALENEMETHANOL 97
• Synonyms: 3-METHOXY-2-NAPHTHALENEMETHANOL 97;5-METHOXY-2-NAPHTHALENEMETHANOL, 97%;(3-Methoxynaphthalen-2-yl)methanol;3-Hydroxy-2-methoxynaphthalene;3-Methoxy-2-naphthalenemethanol 97%
• CAS NO: 39110-92-4
• Molecular Formula: C₁₂H₁₂O₂
• Molecular Weight: 188.22248
• Product Categories: Alcohols;C9 to C30;Oxygen Compounds
• Mol File: 39110-92-4.mol
• Article Data: 1

Chemical Properties

• Melting Point: 70-74 °C(lit.)
• Boiling Point: 347.2 °C at 760 mmHg
• Flash Point: 163.1 °C
• Appearance: /
• Density: 1.166 g/cm³
• Vapor Pressure: 2.06E-05mmHg at 25°C
• Refractive Index: 1.627
• PKA: 13.89±0.10(Predicted)
• CAS DataBase Reference: 3-METHOXY-2-NAPHTHALENEMETHANOL 97(CAS DataBase Reference)
• NIST Chemistry Reference: 3-METHOXY-2-NAPHTHALENEMETHANOL 97(39110-92-4)
• EPA Substance Registry System: 3-METHOXY-2-NAPHTHALENEMETHANOL 97(39110-92-4)

Safety Data

• WGK Germany: 3
• Hazardous Substances Data: 39110-92-4(Hazardous Substances Data)

Usage

Uses

3-Methoxy-2-naphthalenemethanol may be used to synthesize 2-carbomethoxy-4-methoxy-6,7-benzoindole.

InChI:InChI=1/C12H12O2/c1-14-12-7-10-5-3-2-4-9(10)6-11(12)8-13/h2-7,13H,8H2,1H3

Downstream Products

• 61873-80-1 3-methoxy-2-methylnaphthalene 
• 1274918-34-1 2-(4-chlorobenzyl)-3-methoxynaphthalene 
• 562838-51-1 3-Benzhydryl-1-[(3-methoxy-2-naphtyl)methyl]-4-piperidinone 
• 483-55-6 phthiocol 
• 123239-68-9 3-benzyl-2-methoxynaphthalene 
• 123239-70-3 2-benzyloxy-3-hydroxynaphthalene 
• 924904-18-7 (+)-(S)-10,10'-dimethoxy-9,9'-biphenanthryl 
• 443911-29-3 (3-aminooxalyl-1-cyclohexylmethyl-2-methyl-1H-benzo[g]indol-4-yloxy)-acetic acid methyl ester 
• 443911-43-1 1-cyclohexylmethyl-2-carboethoxy-4-methoxybenz[g]indole 

Relevant articles and documents

Controlled photochemical release of nitric oxide from O2-naphthylmethyl- and O2-naphthylallyl-substituted diazeniumdiolates

The photochemistry of O2-naphthylmethyl- and O2-naphthylallyl-substituted diazeniumdiolates has been investigated. Electron-donating methoxy group substitution is shown to have a significant effect on the observed photochemistry, with the appropriate substitution pattern resulting in efficient diazeniumdiolate photorelease. Observed nitric oxide release rates from these photoprecursors are consistent with those expected for normal thermal dissociation of the diazeniumdiolate in aqueous solutions and show the same pH dependence. Copyright