2114-30-9

Basic information

• Product Name: 1-(4-methylphenyl)propyl acetate
• Synonyms: 1-(4-methylphenyl)propyl acetate
• CAS NO: 2114-30-9
• Molecular Weight: 192.258
• Mol File: 2114-30-9.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 1-(4-methylphenyl)propyl acetate(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(4-methylphenyl)propyl acetate(2114-30-9)
• EPA Substance Registry System: 1-(4-methylphenyl)propyl acetate(2114-30-9)

Safety Data

• Hazardous Substances Data: 2114-30-9(Hazardous Substances Data)

Upstream product

• 622-97-9 1-ethenyl-4-methylbenzene 
• 546-67-8 lead(IV) tetraacetate 
• 3240-34-4 [bis(acetoxy)iodo]benzene 
• 104-87-0 4-methyl-benzaldehyde 
• 25574-04-3 1-p-tolyl-1-propanol 
• 108-24-7 acetic anhydride 
• 74-96-4 ethyl bromide 
• 2929-93-3 p-tolylmethylenediacetate 

Relevant articles and documents

Alkene Oxyalkylation Enabled by Merging Rhenium Catalysis with Hypervalent Iodine(III) Reagents via Decarboxylation

Rhenium-catalyzed oxyalkylation of alkenes is described, where hypervalent iodine(III) reagents derived from widely occurring aliphatic carboxylic acids were used as, for the first time, not only an oxygenation source but also an alkylation source via decarboxylation. The reaction also features a wide substrate scope, totally regiospecific difunctionalization, mild reaction conditions, and ready availability of both substrates. Mechanistic studies revealed a decarboxylation/radical-addition/cation-trapping cascade operating in the reaction.

Sonochemical reactions of lead tetraacetate with 4-substituted styrenes

A good linear free energy relationship was observed between the radical reactivity of the sonochemical reactions of 4-substituted styrenes with lead tetraacetate and the vapor pressure of the styrenes, indicating a probable control of the process by an intra-bubble activation.