3412-59-7

Basic information

• Product Name: Silane, trichloro(2-phenylethenyl)-, (E)-
• Synonyms: trichlorosilylstyrene;trans styryl trichloro silane;styryltrichlorosilane;E-1-phenyl-2-trichlorosilylethene;(E)-β-trichlorosilylstyrene;(E)-β-(trichlorosilyl)styrene
• CAS NO: 3412-59-7
• Molecular Formula: C8H7Cl3Si
• Molecular Weight: 237.588
• Mol File: 3412-59-7.mol
• Article Data: 16

Chemical Properties

• Boiling Point: 89-90 °C(Press: 4 Torr)
• Density: 1.292±0.06 g/cm3(Predicted)
• CAS DataBase Reference: Silane, trichloro(2-phenylethenyl)-, (E)-(CAS DataBase Reference)
• NIST Chemistry Reference: Silane, trichloro(2-phenylethenyl)-, (E)-(3412-59-7)
• EPA Substance Registry System: Silane, trichloro(2-phenylethenyl)-, (E)-(3412-59-7)

Safety Data

• Hazardous Substances Data: 3412-59-7(Hazardous Substances Data)

Upstream product

• 536-74-3 phenylacetylene 
• 100-42-5 styrene 
• 75-94-5 trichlorovinylsilane 
• 246047-72-3 tricyclohexylphosphine[1,3-bis(2,4,6-trimethylphenyl)-4,5-dihydroimidazol-2-ylidine][benzylidene]ruthenium(II) dichloride 
• 10025-78-2 trichlorosilane 

Downstream Products

• 125656-14-6 1,2-dibromo-1-(trifluorosilyl)-2-phenylethane 
• 122-78-1 phenylacetaldehyde 
• 406218-90-4 1,2-bis(trichlorosilyl)phenylethane 
• 21673-50-7 (trans-2-phenylethenyl)tris(pentafluorophenyl)silane 
• 1694-19-5 E-1-(phenyl)-2-(4'-methoxyphenyl)ethene 
• 19372-00-0 1-(trimethylsilyl)-2-phenylethene 
• 174279-18-6 (E)-β-(mesityldimethylsilyl)styrene 
• 174279-17-5 (E)-β-<(2,6-dimethylphenyl)dimethylsilyl>styrene 
• 70531-02-1 trans-1-phenyl-2-(trimethoxysilyl)ethene 
• 125656-18-0 l-1,2-dibromo-2-phenyl-1-(trichlorosilyl)ethane 

Relevant articles and documents

Functionalized vinylsilanes via highly efficient and recyclable Pt-nanoparticle catalysed hydrosilylation of alkynes

A mild, selective and facile synthesis of vinylsilanes via a recyclable platinum nanoparticle catalysed hydrosilylation of alkynes is reported. Various functionalized alkynes are selectively hydrosilylated to furnish functional β-E vinylsilanes in high yi

Platinum(0) olefin complexes of a bulky terphenylphosphine ligand. Synthetic, structural and reactivity studies

A novel terphenylphosphine PMe2ArDipp2 (1) (Dipp = 2,6-iPr2C6H3) forms stable Pt(0) complexes with ethene and 3,3-dimethylbut-1-ene that behave as sources of the reactive Pt(PMe

The effect of substituents at silicon on the cross-metathesis of trisubstituted vinylsilanes with olefins

Efficient cross-metathesis of vinylsilanes, carrying a large spectrum of different substituents at silicon, with various olefins in the presence of the first and second generation Grubbs catalyst and Hoveyda-Grubbs catalyst is described. On the basis of the results of equimolar reactions of vinylsilanes with ruthenium alkylidene complexes and experiments with deuterium-labelled reagents, a general, metallacarbene mechanism for the cross-metathesis of trisubstituted vinylsilanes with olefins has been suggested. Reaction was proved to be a valuable method for synthesis of unsaturated organosilicon derivatives.