3139-85-3

Basic information

• Product Name: 4-Ethenylbenzophenone
• Synonyms: 4-Ethenylbenzophenone;4-Vinylbenzophenone;phenyl(4-vinylphenyl)methanone
• CAS NO: 3139-85-3
• Molecular Formula: C₁₅H₁₂O
• Molecular Weight: 208.26
• Mol File: 3139-85-3.mol
• Article Data: 32

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 4-Ethenylbenzophenone(CAS DataBase Reference)
• NIST Chemistry Reference: 4-Ethenylbenzophenone(3139-85-3)
• EPA Substance Registry System: 4-Ethenylbenzophenone(3139-85-3)

Safety Data

• Hazardous Substances Data: 3139-85-3(Hazardous Substances Data)

Upstream product

• 7486-35-3 tri-n-butyl(vinyl)tin 
• 134-85-0 4-chlorobenzophenone 
• 1791-26-0 4-vinyl-benzaldehyde 
• 1074-61-9 (4-vinyl-phenyl)-methanol 
• 103-63-9 1-phenyl-2-bromoethane 
• 98-88-4 benzoyl chloride 
• 2768-02-7 (vinyl)trimethoxylsilane 
• 90-90-4 (4-bromophenyl)(phenyl)methanone 
• 313945-23-2 phenyl-(4-vinyl-phenyl)-methanol 
• 1073-67-2 4-vinylbenzyl chloride 
• 100-47-0 benzonitrile 
• 25772-36-5 4-(β-bromoethyl)benzofenone 
• 108-05-4 vinyl acetate 
• 100-42-5 styrene 

Downstream Products

• 1351272-41-7 (2–(4–vinylphenyl)ethene–1,1,2–triyl)tribenzene 
• 1609584-93-1 (E)-4,4'-(but-1-ene-1,4-diyl)dibenzophenone 
• 1609584-84-0 (E)-4-(4-(4-benzoylphenyl)but-1-en-1-yl)benzonitrile 
• 22410-97-5 (RS)-2-(4-benzoylphenyl)propanoic acid 
• 3139-86-4 (4-ethenylphenyl)diphenyl methanol 

Relevant articles and documents

Control of chain ends of polyesters in polycondensation of AA and BB monomers by use of solid-phase reagent

For selective synthesis of linear polyester having a functional group at one end, polycondensation between 1,4-butanediol (1a) and sebacoyl chloride (2a) and between 1,12-dodecanediol (1b) and isophthaloyl chloride (2b) was conducted in the presence of ox

Copper-Catalyzed Trifluoromethylthio-arylsulfonylation of Styrene Derivatives via the Insertion of Sulfur Dioxide

A copper-catalyzed four-component trifluoromethylthio-arylsulfonylation between styrene derivatives, AgSCF3, aryldiazonium tetrafluoroborates, and ex situ generated sulfur dioxide (from SOgen) is presented. This reaction features mild reaction conditions, good functional group tolerance, a broad substrate scope, good yields, and excellent diastereoselectivity. Preliminary mechanistic studies revealed that a radical process might be involved in this transformation.

Polymer, and mixture or formulation, and organic electronic device containing same, and monomer thereof

Disclosed are a polymer, and a mixture or a formulation and an organic electronic device containing same, and applications thereof, and further a monomer of which the polymer is made; the polymer comprises on its side chain a repeating structure unit E, characterizing in that its S1(E)?T1(E))≤0.35 eV or even less, which may allow the said polymer having thermally activated delayed fluorescence (TADF) property. Thus a TADF polymer suitable for printing processes is provided, thereby reducing OLED manufacturing costs.