74454-29-8

Basic information

• Product Name: 1-cyclohex-3-enylmethyl acetate; methane
• Synonyms: EINECS 277-879-4;1-phenylethyl acetate
• CAS NO: 74454-29-8
• Molecular Formula: C₁₀H₁₈O₂
• Molecular Weight: 168.236
• Mol File: 74454-29-8.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 195.3oC at 760 mmHg
• Flash Point: 80.8oC
• CAS DataBase Reference: 1-cyclohex-3-enylmethyl acetate; methane(CAS DataBase Reference)
• NIST Chemistry Reference: 1-cyclohex-3-enylmethyl acetate; methane(74454-29-8)
• EPA Substance Registry System: 1-cyclohex-3-enylmethyl acetate; methane(74454-29-8)

Safety Data

• Hazardous Substances Data: 74454-29-8(Hazardous Substances Data)

Usage

Usage

Flavoring agent in the food industry

Odor

Sweet and fruity

Presence

Found in various fruits and flowers, contributing to their characteristic aroma

Main component

Natural gas

Upstream product

• 100-50-5 3-Cyclohexene-1-carboxaldehyde 
• 17264-01-6 4-(1-hydroxyethyl)-1-cyclohexene 
• 75-36-5 acetyl chloride 
• 108-24-7 acetic anhydride 
• 100-40-3 4-ethenylcyclohexene 

Downstream Products

• 100-40-3 4-ethenylcyclohexene 

Relevant articles and documents

Diacetoxylation of nonconjugated dienes with TeO2 and the isolation of intermediate organotellurium compounds

Tellurium(IV) oxide (TeO2) reacts with nonconjugated dienes in acetic acid at reflux temperature in the presence of lithium halide or iodine to give the corresponding vic-diacetates in moderate yields.When the reaction is carried out at 80 deg C and the reaction mixture is then reduced with aqueous sodium thiosulfate, bis(β-acetoxyalkyl)ditellurides are isolated as main products.Treatment of the ditellurides with refluxing acetic acid affords the corresponding vic-diacetates in good yields.The expected tellurium containing heterocyclic compounds, such as telluracyclopentanes and telluracyclohexanes, are not formed and/or isolated under the conditions employed.When 4-vinylcyclohexene and limonene are used as dienes in the diacetoxylation reaction, aromatic compounds due to the dehydrogenation of cyclohexene ring are also produced in moderate yields. Keywords: Tellurium; Oxidation; Diolefin; Lithium halide; Iodine; Diacetoxylation