723342-96-9

Basic information

• Product Name: (2E,2'E,2''E)-1,1',1''-(benzene-1,3,5-triyl)tris(3-phenylprop-2-en-1-one)
• Synonyms: (2E,2'E,2''E)-1,1',1''-(benzene-1,3,5-triyl)tris(3-phenylprop-2-en-1-one)
• CAS NO: 723342-96-9
• Molecular Weight: 468.552
• Mol File: 723342-96-9.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: (2E,2'E,2''E)-1,1',1''-(benzene-1,3,5-triyl)tris(3-phenylprop-2-en-1-one)(CAS DataBase Reference)
• NIST Chemistry Reference: (2E,2'E,2''E)-1,1',1''-(benzene-1,3,5-triyl)tris(3-phenylprop-2-en-1-one)(723342-96-9)
• EPA Substance Registry System: (2E,2'E,2''E)-1,1',1''-(benzene-1,3,5-triyl)tris(3-phenylprop-2-en-1-one)(723342-96-9)

Safety Data

• Hazardous Substances Data: 723342-96-9(Hazardous Substances Data)

Upstream product

• 779-90-8 1,3,5-triacetylbenzene 
• 100-52-7 benzaldehyde 
• 14604-31-0 (E)-1-phenylpent-1-en-4-yn-3-ol 
• 824-79-3 sodium 4-methylbenzenesulfinate 

Relevant articles and documents

Silver(I)-Promoted Radical Sulfonylation of Allyl/Propargyl Alcohols: Efficient Synthesis of γ-Keto Sulfones

An efficient Ag2CO3-promoted sulfonylation of allyl/propargyl alcohols with sodium sulfinates has been developed. The reaction tolerates a wide range of functional groups to deliver γ-keto sulfones in high yields (up to 93 %). Propargyl alcohols furnished trimerization product 1,3,5-triaroylbenzenes in the presence of sodium methanesulfinate under the standard conditions. A mechanism involving a sulfonyl radical was suggested.