130255-49-1

Basic information

• Product Name: Silane, ethenylidenebis[dimethylphenyl-
• CAS NO: 130255-49-1
• Molecular Formula: C18H24Si2
• Molecular Weight: 296.56
• Mol File: 130255-49-1.mol
• Article Data: 10

Chemical Properties

• CAS DataBase Reference: Silane, ethenylidenebis[dimethylphenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Silane, ethenylidenebis[dimethylphenyl-(130255-49-1)
• EPA Substance Registry System: Silane, ethenylidenebis[dimethylphenyl-(130255-49-1)

Safety Data

• Hazardous Substances Data: 130255-49-1(Hazardous Substances Data)

Upstream product

• 824985-52-6 2,2,4,4-tetramethyl-3-methylene-1,5-dioxa-2,4-disilacycloheptane 
• 50-00-0 formaldehyd 
• 27628-30-4 tris(phenyldimethylsilyl)methane 
• 766-77-8 Dimethylphenylsilane 
• 17156-64-8 (dimethylphenylsilyl)acetylene 
• 1125-26-4 dimethylphenylvinylsilane 
• 768-56-9 4-Phenylbut-1-ene 
• 130255-42-4 bis(methylthio)bis(dimethylphenylsilyl)methane 
• 130255-43-5 bis(dimethyl(phenyl)silyl)methanone 
• 147609-35-6 dibromobis(dimethylphenylsilyl)methane 
• 768-33-2 phenyldimethylsilyl chloride 
• 824985-51-5 1,2-bis(dimethylvinylsilyloxy)ethane 
• 443285-84-5 1-bromo-1,1-bis(dimethylphenylsilyl)ethane 
• 19493-09-5 Methylenetriphenylphosphorane 

Downstream Products

• 431990-78-2 6,6-bis(dimethylphenylsilyl)tetradecane 
• 1026012-15-6 C₅₂H₈₂Si₄ 
• 1026449-77-3 C₂₉H₄₀Si₂ 

Relevant articles and documents

A facile synthesis of 1,1-bis(silyl)ethenes

(Chemical Equation Presented). Symmetrical 1,1-bis(silyl)ethenes have been easily prepared via ruthenium complex-catalyzed silylative coupling cyclization of 1,2-bis(dimethylvinylsiloxy)ethane to give 2,2,4,4-tetramethyl-3-methylene-1, 5-dioxa-2,4-disilac

Phosphine-stabilized, oxide-supported rhodium catalysts for highly efficient silylative coupling reactions

Oxide-supported rhodium catalysts with excellent activity in silylative coupling reactions have been developed. Reductive pretreatment of the catalysts in the presence of 0.5 equiv triphenylphosphine under a hydrogen atmosphere enhanced and stabilized the

Shuffle off the classic β-Si elimination by Ni-NHC cooperation: Implication for C-C forming reactions involving Ni-alkyl-β-silanes

Via a cooperation of NHC, Si substituents and a M center, β-Si elimination was attenuated, revealing a new way to attain a high Ni-β-SiR3:Ni-σ-SiR3 ratio. The scope is illustrated by a head-to-tail vinylsilane-α-olefin hydroalkenylation.