13128-74-0

Basic information

• Product Name: 4,4-DIPHENYL-CYCLOHEXANE-1,3-DIONE
• Synonyms: 4,4-DIPHENYL-CYCLOHEXANE-1,3-DIONE
• CAS NO: 13128-74-0
• Molecular Formula: C₁₈H₁₆O₂
• Molecular Weight: 264.32
• Mol File: 13128-74-0.mol
• Article Data: 4

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 4,4-DIPHENYL-CYCLOHEXANE-1,3-DIONE(CAS DataBase Reference)
• NIST Chemistry Reference: 4,4-DIPHENYL-CYCLOHEXANE-1,3-DIONE(13128-74-0)
• EPA Substance Registry System: 4,4-DIPHENYL-CYCLOHEXANE-1,3-DIONE(13128-74-0)

Safety Data

• Hazardous Substances Data: 13128-74-0(Hazardous Substances Data)

Upstream product

• 781-35-1 1,1-diphenylacetone 
• 140-88-5 ethyl acrylate 
• 119-61-9 benzophenone 

Downstream Products

• 75010-96-7 3-methoxy-6,6-diphenylcyclohex-2-ene-1-one 
• 75010-97-8 3-methoxy-4,4-diphenylcyclohex-2-en-1-one 
• 4528-64-7 4,4-diphenyl-2-cyclohexen-1-one 
• 184677-78-9 (3aR,7R,7aR)-7-Fluoro-4,4-diphenyl-octahydro-isoindole 
• 146402-78-0 (3aR,7R,7aR)-4,4-diphenyl-7-fluoro-2-tert-butyloxycarbonylperhydroisoindole 
• 675571-69-4 (3ARS,7ARS)-7,7-diphenyl-4-perhydroisoindolone 
• 135910-95-1 (3aR,7aR)-7,7-Diphenyl-octahydro-isoindol-4-one 
• 146402-73-5 (3aR,7S,7aR)-7-Hydroxy-4,4-diphenyl-octahydro-isoindole-2-carboxylic acid tert-butyl ester 
• 146402-84-8 1-((3aR,7R,7aR)-7-Fluoro-4,4-diphenyl-octahydro-isoindol-2-yl)-2-[2-(3-pyrrolidin-1-yl-propoxy)-phenyl]-ethanone 
• 86396-20-5 4,4-Diphenyl-cyclohexane-1,2,3-trione 
• 73982-28-2 6,6-diphenylcyclohex-2-en-1-one 
• 17429-38-8 3-methyl-4,4-diphenylcyclohex-2-ene-1-one 
• 103367-59-5 3-methyl-4,4-diphenylcyclohex-2-ene-1-one tosylhydrazone 
• 103367-60-8 3-methyl-4,4-diphenylcyclohex-1-ene 

Relevant articles and documents

Synthesis of 1,3-Cycloalkadienes from Cycloalkenes: Unprecedented Reactivity of Oxoammonium Salts

Few methods allow for the direct conversion of cycloalkenes into cycloalkadienes with high chemo- and regioselectivity. Herein, we report a convenient one-pot process for this transformation that involves the unprecedented N-preferential group transfer of N-oxoammonium salts to cycloalkenes, followed by Cope elimination, to afford cycloalkadienes at room temperature and pressure.

Expedient enantiospecific synthesis of RP 73613: A new selective non-peptide NK1 antagonist

The synthesis of RP 73613 was achieved in 13 steps with an overall yield of 12%. The strategy was based on a [3 + 2] azomethine ylid dipolar cycloaddition to generate the bicyclic framework and the asymmetric was introduced by resolution.