86561-30-0

Basic information

• Product Name: 1-(4-methylphenyl)ethyl acetate
• CAS NO: 86561-30-0
• Molecular Formula: C₁₁H₁₄O₂
• Molecular Weight: 178.231
• Mol File: 86561-30-0.mol
• Article Data: 28

Chemical Properties

• Boiling Point: 233.6°Cat760mmHg
• Flash Point: 94.6°C
• Density: 1.013g/cm³
• CAS DataBase Reference: 1-(4-methylphenyl)ethyl acetate(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(4-methylphenyl)ethyl acetate(86561-30-0)
• EPA Substance Registry System: 1-(4-methylphenyl)ethyl acetate(86561-30-0)

Safety Data

• Hazardous Substances Data: 86561-30-0(Hazardous Substances Data)

Upstream product

• 536-50-5 CH₃C₆H₄CH(CH₃)OH 
• 64-19-7 acetic acid 
• 75-89-8 2,2,2-trifluoroethanol 
• 2362-36-9 1-(1-chloroethyl)-4-methylbenzene 
• 127-09-3 sodium acetate 
• 1186-52-3 tetradeuterioacetic acid 
• 67609-56-7 1-ethyl-4-methyl-4-nitrocyclohexa-2,5-dienyl acetate 
• 622-96-8 4-methylethylbenzene 
• 127-08-2 potassium acetate 
• 2929-93-3 p-tolylmethylenediacetate 
• 108-22-5 Isopropenyl acetate 
• 108-58-7 Resorcinol diacetate 
• 108-05-4 vinyl acetate 
• 108-24-7 acetic anhydride 

Downstream Products

• 42070-92-8 (R)-1-(4-methylphenyl)ethanol 
• 19759-40-1 (S)-1-(4-methylphenyl)ethanol acetate 
• 536-50-5 (S)-1-(4-Methylphenyl)ethanol 
• 1016538-33-2 2-(1-(p-tolyl)ethyl)cyclopentan-1-one 
• 91633-31-7 1-(para-methylphenyl)-1-azidoethane 

Relevant articles and documents

Highly enantioselective hydrogenation of cyclic enol acetates catalyzed by a Rh - PennPhos complex

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Base-catalyzed selective esterification of alcohols with unactivated esters

A practical and efficient base-catalyzed esterification has been developed for the facile synthesis of a broad range of esters from simple alcohols with unactivated tert-butyl esters. This protocol could be conducted at mild conditions, providing esters in high to excellent yields with good functional tolerance. Mechanistic studies provided evidence of an exchange of the tert-butyl alkoxide metal with the alcohol, producing a new alkoxide to participate in the transesterification reaction.

Enhancement of (stereo)selectivity in dynamic kinetic resolution using a core-shell nanozeolite@enzyme as a bi-functional catalyst

A core-shell nanozeolite@enzyme bi-functional catalyst is constructed, which greatly improves selectivity and stereoselectivity of products in dynamic kinetic resolution of aromatic secondary alcohols compared with mixed catalysts, especially those involving small acyl donors. This journal is the Partner Organisations 2014.