7459-73-6

Upstream product

• 1073-67-2 4-vinylbenzyl chloride 
• 75-78-5 dimethylsilicon dichloride 

Downstream Products

• 2156-04-9 4-Vinylphenylboronic acid 
• 106340-07-2 3-Methyl-4-(4-vinyl-phenyl)-[1,2,5]thiadiazole 
• 360068-90-2 (S)-(-)-α,α-di(4-vinylphenyl)-2-[(N-ethoxycarbonyl)pyrrolidine]methanol 
• 92908-08-2 bis-(4-vinyl-phenyl)-mercury 
• 48187-95-7 {4-(C₆H₅)2SbC₆H₄CHCH₂}x 
• 100409-87-8 {(C₆H₅)2BiC₆H₄-p-CHCH₂}n 
• 1015-17-4 (C₂H₅)3SnC₆H₄-p-CHCH₂ 
• 2177-14-2 (C₆H₅)3SnC₆H₄-p-CHCH₂ 
• 2413-03-8 (4-vinylphenyl)tricyclohexyltin 
• 802-03-9 tris(4-vinylphenyl)bismuthine 
• 16396-62-6 2,4,6-tris-(4-vinylphenyl)cyclotriboroxane 
• 47604-04-6 (C₆H₅)2Sn(C₆H₄-p-CHCH₂)2 
• 108188-56-3 bis(η-(4-vinylphenyl)benzene)molybdenum 
• 107278-31-9 (C₆H₅)2Sn(C₆H₄-p-CH₂CH₂Sn(C₆H₅)3)2 

Relevant academic research and scientific papers

A chemically inert hydrophilic resin for solid phase organic synthesis

A new mechanically stable and chemically inert resin for solid phase organic synthesis is described. The resin, POEPS-3 (1), is prepared by bulk and inverse suspension radical polymerisation of macromonomers consisting of polyethylene glycol 1500 partiall

Living anionic polymerization of 4-(α-alkylvinyl)styrene derivatives

The anionic polymerization of four bis-functionalized styrene derivatives with α-alkylvinyl groups have been carried out in THF at -78°C with the initiator prepared from oligo(α-methylstyryl)lithium and potassium tert-butoxide. The four monomers herein us

Immobilization of chiral ligands on polymer fibers by electron beam induced grafting and applications in enantioselective catalysis

(Equation presented) Styrenic TADDOL and L-prolinol-derived monomers were immobilized on polyethylene fibers by electron beam induced preirradiation grafting using styrene as comonomer. The polymer-supported chiral ligands were utilized as catalysts in th

Diphenylsiloxane oligomers functionalized at both terminal and method for the preparation thereof

There is disclosed a diphenylsiloxane oligomer functionalized at both terminals, and methods for the preparation thereof, said oligomer having the following general formula G-(OSi(Ph)2)m O--G wherein Ph denotes a phenyl radical, m is 3 to 50 and G is has a formula independently selected from the group consisting of STR1 in which R1 is independently selected from the group consisting of hydrogen and a monovalent hydrocarbon group having 2 to 8 carbon atoms, said monovalent hydrocarbon group excluding phenyl, tolyl, xylyl, and ethylphenyl radicals, R is independently selected from the group consisting of R1, methyl radical and phenyl radical, Q is a divalent hydrocarbon group and n is an integer having a value of 1 to 3.