141211-14-5

Basic information

• Product Name: 4-acetyl-1,3-diphenylhexane-1,5-dione
• CAS NO: 141211-14-5
• Molecular Weight: 308.377
• Mol File: 141211-14-5.mol
• Article Data: 19

Chemical Properties

• CAS DataBase Reference: 4-acetyl-1,3-diphenylhexane-1,5-dione(CAS DataBase Reference)
• NIST Chemistry Reference: 4-acetyl-1,3-diphenylhexane-1,5-dione(141211-14-5)
• EPA Substance Registry System: 4-acetyl-1,3-diphenylhexane-1,5-dione(141211-14-5)

Safety Data

• Hazardous Substances Data: 141211-14-5(Hazardous Substances Data)

Upstream product

• 123-54-6 acetylacetone 
• 614-47-1 1,3-diphenyl-propen-3-one 
• 94-41-7 benzalacetophenone 

Downstream Products

• 10346-08-4 3,5-diphenylcyclohex-2-en-1-one 
• 51522-42-0 6-acetyl-3,5-diphenyl-2-cyclohexen-1-one 

Relevant articles and documents

Cerium catalyzed michael addition of 1,3-dicarbonyl compounds under microwave irradiation

Cerium chloride heptahydrate proves to be an efficient catalyst for Michael addition of 1,3-dicarbonyl compounds, through a simple solvent free reaction under microwave irradiations.

Phase-transfer catalyzed Michael addition reaction using a new C 2-symmetric quaternary ammonium salt derived from l-proline

A new C2-symmetric quaternary ammonium salt easily prepared from l-proline, was developed and used as an efficient phase-transfer catalyst (PTC) in Michael addition reaction of various active methylene compounds to aromatic enones. Malonate est

Dual catalysis of the Michael reaction

The Michael reaction, with conjugate bases of β-diketones as donors and with α,β-unsaturated ketones as acceptors, is efficiently catalyzed by a combination of clay-supported nickel bromide (heterogeneous) and ferric chloride (homogeneous).

Ba(OH)2 AS CATALYST IN ORGANIC REACTIONS-PART XVI-CONTRIBUTION TO THE STUDY OF THE MICHAEL ADDITION MECHANISM TO CHALCONE IN INTERFACIAL SOLID-LIQUID CONDITIONS

The Michael addition of several active methylene compounds to chalcone, catalyzed in interfacial solid-liquid conditions is described.The mechanism of the process is analyzed using the Michael addition of diethyl malonate to chalcone as the reaction test.

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

Synthesis of biphenyl-based ligand: Application in copper-mediated chemoselective michael reaction

A biphenyl-based ligand attached was synthesized and screened in copper-mediated Michael reaction. The catalyst system works well with carbon or sulfur nucleophiles as Michael donors and cyclohexenone or chalcones as the acceptors under mild and neutral r