1006715-23-6

Basic information

• Product Name: dimethyl(phenyl)(4-(trifluoromethyl)phenyl)silane
• Synonyms: dimethyl(phenyl)(4-(trifluoromethyl)phenyl)silane
• CAS NO: 1006715-23-6
• Molecular Weight: 280.365
• Mol File: 1006715-23-6.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: dimethyl(phenyl)(4-(trifluoromethyl)phenyl)silane(CAS DataBase Reference)
• NIST Chemistry Reference: dimethyl(phenyl)(4-(trifluoromethyl)phenyl)silane(1006715-23-6)
• EPA Substance Registry System: dimethyl(phenyl)(4-(trifluoromethyl)phenyl)silane(1006715-23-6)

Safety Data

• Hazardous Substances Data: 1006715-23-6(Hazardous Substances Data)

Upstream product

• 402-43-7 p-trifluoromethylphenyl bromide 
• 185990-03-8 dimethylphenyl(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)silane 
• 1246260-87-6 N,N,N-trimethyl-4-(trifluoromethyl)benzeneaminium trifluoromethanesulfonate 
• 1234935-78-4 (dimethyl(phenyl)silyl)zinc chloride 
• 145963-47-9 1-(methylsulfinyl)-4-(trifluoromethyl)benzene 
• 766-77-8 Dimethylphenylsilane 
• 27389-56-6 N,N,N-trimethyl-4-(trifluoromethyl)benzenaminium iodide 
• 455-13-0 4-Iodobenzotrifluoride 
• 3839-31-4 dimethyl(phenyl)silyl lithium 
• 98-56-6 4-chlorobenzotrifluoride 
• 544-97-8 dimethyl zinc(II) 
• 141738-80-9 2-chloro-1-iodo-4-(trifluoromethyl)benzene 

Relevant articles and documents

Dimethylformamide-stabilised palladium nanoclusters catalysed coupling reactions of aryl halides with hydrosilanes/disilanes

N,N-Dimethylformamide-stabilised Pd nanocluster (NC) catalysed cross-coupling reactions of hydrosilane/disilane have been investigated. In this reaction, the coupling reaction proceeds without ligands with low catalyst loading. N,N-Dimethylacetamide is a crucial solvent in these reactions. The solvent effect was considered by various techniques, such as transmission electron microscopy, X-ray photoelectron spectroscopy, and thermogravimetric analysis. The Pd NCs can be recycled five times under both hydrosilane and disilane reaction conditions.

A nickel-catalyzed silylation reaction of alkyl aryl sulfoxides with silylzinc reagents

Ni(PEt3)Cl2-catalyzed silylation of alkyl aryl sulfoxides with silylzinc reagents was carried out. This protocol allows alkyl aryl sulfoxides to convert to arylsilicon compounds under mild reaction conditions, tolerates a range of functional groups and is suitable for a wide scope of substrates.

Arylsilylation of aryl halides using the magnetically recyclable bimetallic Pd-Pt-Fe3O4 catalyst

Transition metal-catalyzed silylations have typically involved the use of homogeneous non-recyclable catalytic systems. In this work, the first example of a recyclable catalytic system for the synthesis of arylsilanes has been reported, which utilizes the