2097-02-1

Basic information

• Product Name: Silane, dimethylbis(4-methylphenyl)-
• CAS NO: 2097-02-1
• Molecular Formula: C16H20Si
• Molecular Weight: 240.42
• Mol File: 2097-02-1.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: Silane, dimethylbis(4-methylphenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Silane, dimethylbis(4-methylphenyl)-(2097-02-1)
• EPA Substance Registry System: Silane, dimethylbis(4-methylphenyl)-(2097-02-1)

Safety Data

• Hazardous Substances Data: 2097-02-1(Hazardous Substances Data)

Upstream product

• 2417-95-0 p-tolyllithium 
• 75-78-5 dimethylsilicon dichloride 
• 1432-39-9 dimethyl-p-tolylsilane 
• 106-43-4 para-chlorotoluene 
• 106-38-7 para-bromotoluene 
• 74-88-4 methyl iodide 

Downstream Products

• 849534-01-6 bis[4-(diethoxyphosphoryl)methyl]phenyldimethylsilane 
• 17002-99-2 bis(4-hydroxymethylphenyl)dimethylsilane 
• 18537-52-5 me2Si(ph-4-COOme)2 
• 16117-02-5 Dimethyl-bis-<4-brommethyl-phenyl>-silan 
• 67592-77-2 Bromodimethyl(4-methylphenyl)silane 
• 17003-01-9 4,4′-(dimethylsilanediyl)bis-benzoic acid 

Relevant articles and documents

METHOD FOR PRODUCING ARYLSILANE COMPOUND CONTAINING HALOSILANE COMPOUND AS RAW MATERIAL

PROBLEM TO BE SOLVED: To provide a method for producing an arylsilane compound with low production cost. SOLUTION: A method for producing an arylsilane compound includes a reaction step for the cross-coupling reaction of a halosilane compound represented by general formula (A-1), (A-2), or (A-3) and an arylboronic acid pinacol ester in the presence of a nickel catalyst, a Lewis acid catalyst, and an organic base (R independently represent an aromatic hydrocarbon group, a heteroaromatic ring group, or a C1-20 hydrocarbon group; X independently represent a halogeno group or a trifluoromethanesulfonyloxy group). SELECTED DRAWING: None COPYRIGHT: (C)2020,JPOandINPIT

B(C6F5)3-Catalyzed C-Si/Si-H Cross-Metathesis of Hydrosilanes

The substituent redistribution of hydrosilanes on silicon through C-Si and Si-H bond cleavage and reformation is of great interest and importance, but this transformation is usually difficult to achieve in a selective fashion. By using electron-rich aromatic hydrosilanes, we have achieved for the first time the selective C-Si/Si-H bond homo- and cross-metathesis of a series of hydrosilanes in the presence of a boron catalyst B(C6F5)3. This protocol features simple reaction conditions, high chemoselectivity, wide substrate scope, and high functionality tolerance, offering a new pathway for the synthesis of multisubstituted functional silanes.

Synthesis, photophysical and electrochemical properties of symmetric silicon-linked coumarin-oxadiazole derivatives

A novel, silicon-linked, symmetric, V-shaped, coumarin derivative (1) with an electron-deficient 1,3,4-oxadiazoles unit and a phenyl moiety was synthesized and characterized. An efficient multifunctional organic light-emitting diode material was obtained