133616-31-6

Basic information

• Product Name: phenyl 3-phenyl-1-propenyl sulfone
• Synonyms: phenyl 3-phenyl-1-propenyl sulfone
• CAS NO: 133616-31-6
• Molecular Formula: C₁₅H₁₄O₂S
• Molecular Weight: 258.33546
• Mol File: 133616-31-6.mol
• Article Data: 5

Chemical Properties

• Appearance: /
• CAS DataBase Reference: phenyl 3-phenyl-1-propenyl sulfone(CAS DataBase Reference)
• NIST Chemistry Reference: phenyl 3-phenyl-1-propenyl sulfone(133616-31-6)
• EPA Substance Registry System: phenyl 3-phenyl-1-propenyl sulfone(133616-31-6)

Safety Data

• Hazardous Substances Data: 133616-31-6(Hazardous Substances Data)

Upstream product

• 100-51-6 benzyl alcohol 
• 56069-39-7 diethyl phenylsulfonylmethylphosphonate 
• 122-78-1 phenylacetaldehyde 
• 133616-25-8 2-(1-Benzenesulfonyl-3-phenyl-propylsulfanyl)-pyridine 
• 35249-73-1 benzyl chlorooxalate 
• 300-57-2 allylbenzene 
• 5535-48-8 PVS 

Relevant articles and documents

Chloro-substituted Hoveyda-Grubbs ruthenium carbene: Investigation of electronic effects

A series of applications of cross and ring-closing metathesis has been made to investigate the application profile of the chloro-substituted Hoveyda-Grubbs ruthenium carbene in order to evaluate electronic effects resulting from the introduction of a chlorine atom para to the isopropoxy moiety of its parent catalyst.

Nitro-substituted Hoveyda-Grubbs ruthenium carbenes: Enhancement of catalyst activity through electronic activation

The design, synthesis, stability, and catalytic activity of nitro-substituted Hoveyda-Grubbs metathesis catalysts are described. The highly active and stable meta- and para-substituted complexes are attractive from a practical point of view. These catalys

Conversion of Hydroxyl Groups in Alcohols to Other Functional Groups with N-Hydroxy-2-thiopyridone, and Its Application to Dialkylamines and Thiols

The radical decarboxylation reaction of N-alkoxyoxalyloxy-2-thiopyridone which was prepared by the reaction of alcohol, oxalyl chloride, and N-hydroxy-2-thiopyridone was studied both in the absence and presence of olefinic compounds.The same reactions with olefinic and acetylenic alcohols gave the corresponding lactone derivatives.On the other hand the unsymmetrical alkyl 2-pyridyl disulfides were obtained by the same reaction with aliphatic thiols.