1261085-79-3

Basic information

• Product Name: 5-benzoyl-6-methyl-4-phenyl-3,4-dihydro-2H-pyran-2-one
• Synonyms: 5-benzoyl-6-methyl-4-phenyl-3,4-dihydro-2H-pyran-2-one
• CAS NO: 1261085-79-3
• Molecular Weight: 292.334
• Mol File: 1261085-79-3.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 5-benzoyl-6-methyl-4-phenyl-3,4-dihydro-2H-pyran-2-one(CAS DataBase Reference)
• NIST Chemistry Reference: 5-benzoyl-6-methyl-4-phenyl-3,4-dihydro-2H-pyran-2-one(1261085-79-3)
• EPA Substance Registry System: 5-benzoyl-6-methyl-4-phenyl-3,4-dihydro-2H-pyran-2-one(1261085-79-3)

Safety Data

• Hazardous Substances Data: 1261085-79-3(Hazardous Substances Data)

Upstream product

• 2579-22-8 Phenylpropargyl aldehyde 
• 93-91-4 1-phenylbutan-1,3-dione 
• 5443-49-2 α-bromocinnamaldehyde 
• 66894-04-0 2,3-dibromo-3-phenyl propanal 
• 104-55-2 3-phenyl-propenal 
• 14371-10-9 (E)-3-phenylpropenal 

Downstream Products

• 99512-42-2 methyl 5-oxo-3-phenylhexanoate 
• 77565-69-6 methyl 5-oxo-3,5-diphenylpentanoate 

Relevant articles and documents

Polyhalides as Efficient and Mild Oxidants for Oxidative Carbene Organocatalysis by Radical Processes

Simple and inexpensive polyhalides (CCl4 and C2Cl6) have been found to be effective and versatile oxidants in removing electrons from Breslow intermediates under N-heterocyclic carbene (NHC) catalysis. This oxidative react

Nhc-catalyzed michael addition to α,β-unsaturated aldehydes by redox activation

Through oxidative carbene catalysis the reactivity of enals can be reversed at the β position from the typical electrophilic to nucleophilic (homoenolate chemistry) further to electrophilic reactivity by two consecutive umpolung processes. These redox-act