13098-88-9

Basic information

• Product Name: Acetic acid (1-naphtyl)methyl ester
• Synonyms: 1-Naphthalenemethanol acetate;Acetic acid (1-naphtyl)methyl ester;Acetic acid (1-naphtylmethyl) ester
• CAS NO: 13098-88-9
• Molecular Formula: C₁₃H₁₂O₂
• Molecular Weight: 0
• Mol File: 13098-88-9.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 314.6°C at 760 mmHg
• Flash Point: 143.5°C
• Appearance: /
• Density: 1.135g/cm³
• Vapor Pressure: 0.00046mmHg at 25°C
• Refractive Index: 1.596
• CAS DataBase Reference: Acetic acid (1-naphtyl)methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Acetic acid (1-naphtyl)methyl ester(13098-88-9)
• EPA Substance Registry System: Acetic acid (1-naphtyl)methyl ester(13098-88-9)

Safety Data

• Hazardous Substances Data: 13098-88-9(Hazardous Substances Data)

Usage

InChI:InChI=1/C13H12O2/c1-10(14)15-9-12-7-4-6-11-5-2-3-8-13(11)12/h2-8H,9H2,1H3

Upstream product

• 64-19-7 acetic acid 
• 90-12-0 1-Methylnaphthalene 
• 70755-03-2 (1,2,3,4-tetrahydronaphthalen-1-yl)methyl acetate 

Downstream Products

• 71843-68-0 stearic acid-[1]naphthylmethyl ester 
• 1127-76-0 1-ethylnapthelene 
• 5903-23-1 1-(methoxymethyl)naphthalene 
• 64-19-7 acetic acid 
• 6343-54-0 N-benzylformamide 
• 16413-71-1 N,N-dimethyl(naphthalen-1-yl)methanamine 
• 90-12-0 1-Methylnaphthalene 
• 86-87-3 naphth-1-yl acetic acid 
• 20204-73-3 1-(2-methylbenzyl)naphthalene 
• 20204-71-1 α-(4-methylbenzyl)naphthalene 
• 2876-78-0 methyl 1-naphthylacetate 
• 4780-79-4 1-naphthalene methanol 
• 15374-45-5 1,2-di(1-naphthyl)ethane 
• 33744-50-2 3-(1-naphthyl)-2-propanone 

Relevant articles and documents

Reactions of alkylarenes, benzyl alcohols, sulfides, and phosphine with manganese(III) acetate-chloride ions

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The Liquid-phase Oxidation of the Methylbenzenes by the Cobalt-Copper-Bromide System

The liquid-phase oxidation of the methylbenzenes catalyzed by a catalyst system composed of cobalt(II) and copper(II) acetates and sodium bromide was carried out in the acetic acid at 150 deg C.The corresponding benzyl acetates and benzaldehydes were obtained in high selectivities in most cases.A nuclear-brominated product, i.e., 3-bromo-4-methoxytoluene was also obtained in the oxidation of p-methoxytoluene, wich has two different reaction sites, i.e., o-positions to the electron-donating methoxyl substituent and the benzyl position.However, the substitution of the bromide ion for the acetate ion in the catalyst system gave satisfactory selectivities for the side-chain oxidation products.In the p-xylene oxidation, α,α'-diacetoxy-p-xylene and p-(acetoxymethyl)benzoic acid were also obtained, as well as p-methylbenzyl acetate, though their amounts were small.The oxidation of polymethylbenzenes was also carried out.