53852-96-3

Usage

Type of compound

Diketone

Structure

Cyclohexane ring with a phenyl group attached to the carbon atoms

Potential applications

Intermediate in the synthesis of pharmaceuticals and other organic compounds

Other uses

Production of fragrances, dyes, and other industrial products

Safety concerns

Hazardous if not properly managed

Reactivity

Unique structure and reactivity due to the presence of the diketone group and phenyl groups

Upstream product

• 504-02-9 1,3-cylohexanedione 
• 94-41-7 benzalacetophenone 
• 110-89-4 piperidine 
• 614-47-1 1,3-diphenyl-propen-3-one 

Downstream Products

• 59649-47-7 2,4-diphenyl-5-oxo-5,6,7,8-tetrahydro-4H-chromene 
• 99878-98-5 oxime of 2,4-diphenyl-5-oxo-5,6,7,8-tetrahydroquinoline 
• 99879-01-3 oxime of 2,3-diphenyl-5-oxo-5,6,7,8-tetrahydroquinoline 
• 130716-50-6 2,4-diphenyl-4,6,7,8-tetrahydroquinolin-5(1H)-one 
• 82315-12-6 2,4-Dicyclohexyl-octahydro-chromene 
• 72567-24-9 2,4-Diphenyl-octahydro-chromene 
• 53853-00-2 2,4-diphenyl-5-oxo-5,6,7,8-tetrahydro-4H-thiochromene 
• 72567-19-2 2,4-diphenyl-5-oxo-1-bicyclo<4.4.0>dec-9-ene 
• 504-02-9 1,3-cylohexanedione 
• 94-41-7 benzalacetophenone 
• 62811-59-0 2,3-Diphenyl-5-oxo-5,6,7,8-tetrahydroquinoline 
• 99422-81-8 2,4-diphenyl-7,8-dihydro-6H-quinolin-5-one 
• 84725-12-2 2-(1,3-diphenyl-3-oxopropyl)-1-acetoxy-1-cyclohexene-3-one 

Relevant academic research and scientific papers

Reaction between Chalcones, 1,3-Dicarbonyl Compounds, and Elemental Sulfur: A One-Pot Three-Component Synthesis of Substituted Thiophenes

A simple and atom-economic synthesis of highly substituted thiophenes is demonstrated. Heating a solution of a chalcone and a linear/cyclic 1,3-dicarbonyl compound with elemental sulfur in CH 3 CN in the presence of NEt 3 at 80 °C af

Aqueous Iodine(III)-mediated stereoselective oxidative cyclization for the synthesis of functionalized fused dihydrofuran derivatives

("Figure Presented") An efficient aqueous oxidative cyclization mediated by the combination of iodosobenzene with tetra-(n-butyl)ammonium iodide provides a new convenient and useful route to functionalized fused dihydrofuran derivatives in moderate to excellent yields with high diastereoselectivities.