30436-97-6

Basic information

• Product Name: ((4-(tert-butyl)phenyl)(phenyl)methyl)trimethylsilane
• Synonyms: ((4-(tert-butyl)phenyl)(phenyl)methyl)trimethylsilane
• CAS NO: 30436-97-6
• Molecular Weight: 296.528
• Mol File: 30436-97-6.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: ((4-(tert-butyl)phenyl)(phenyl)methyl)trimethylsilane(CAS DataBase Reference)
• NIST Chemistry Reference: ((4-(tert-butyl)phenyl)(phenyl)methyl)trimethylsilane(30436-97-6)
• EPA Substance Registry System: ((4-(tert-butyl)phenyl)(phenyl)methyl)trimethylsilane(30436-97-6)

Safety Data

• Hazardous Substances Data: 30436-97-6(Hazardous Substances Data)

Upstream product

• 253185-03-4 tert-butylbenzene 
• 17876-95-8 (trimethylsilyl)phenylmethanol 
• 123324-71-0 p-tert-butylphenylboronic acid 
• 591-50-4 iodobenzene 

Relevant articles and documents

Metal-free synthesis of gem -silylboronate esters and their Pd(0)-catalyzed cross-coupling with aryliodides

A transition-metal-free method for the synthesis of gem-silylboronate esters with arylboronic acids and trimethylsilyldiazomethane (TMSCHN2) has been developed. This transformation is a straightforward homologation of arylboronic acids and features wide substrate scope and good functional-group tolerance. The gem-silylboronate esters undergo efficient Suzuki-Miyaura cross-coupling with aryliodides and the silyl group of the product can be further functionalized. Tertiary carbon centers with different substituents can be constructed successfully by selective and sequential functionalization.