139039-99-9

Basic information

• Product Name: Disilane, 1,2-bis(2,4,6-trimethylphenyl)-
• CAS NO: 139039-99-9
• Molecular Formula: C18H26Si2
• Molecular Weight: 298.575
• Mol File: 139039-99-9.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: Disilane, 1,2-bis(2,4,6-trimethylphenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Disilane, 1,2-bis(2,4,6-trimethylphenyl)-(139039-99-9)
• EPA Substance Registry System: Disilane, 1,2-bis(2,4,6-trimethylphenyl)-(139039-99-9)

Safety Data

• Hazardous Substances Data: 139039-99-9(Hazardous Substances Data)

Upstream product

• 120578-34-9 (2,4,6-trimethylphenyl)silane 
• 2633-66-1 2-mesitylmagnesium bromide 
• 198883-34-0 chloro(mesityl)silane 

Downstream Products

• 20536-13-4 1,2-dichlorodisilane 

Relevant articles and documents

Iridium Pincer Catalysts for Silane Dehydrocoupling: Ligand Effects on Selectivity and Activity

Catalytic reactions of bisphosphinite pincer-ligated iridium compounds p-XR(POCOP)IrHCl (POCOP) [2,6-(R2PO)2C6H3, R = iPr, X = H (1); R = tBu, X = COOMe (2); = H (3); = NMe2 (4)] with primary and secondary silanes have been performed. Complex 1 is primarily a silane redistribution precatalyst, but dehydrocoupling catalysis is observed for sterically demanding silane substrates or with aggressive removal of H2. The bulkier compounds (2-4) are silane dehydrocoupling precatalysts that also undergo competitive redistribution with less hindered substrates. Products generated from reactions utilizing 2-4 include low molecular weight oligosilanes with varying degrees of redistribution present or disilanes when employing more sterically demanding silane substrates. Selectivity for redistribution versus dehydrocoupling depends on the steric and electronic environment of the metal but can also be affected by reaction conditions. (Chemical Equation Presented).