4405-40-7

Basic information

• Product Name: Silane, trimethyl[3-(trifluoromethyl)phenyl]-
• CAS NO: 4405-40-7
• Molecular Formula: C10H13F3Si
• Molecular Weight: 218.294
• Mol File: 4405-40-7.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Silane, trimethyl[3-(trifluoromethyl)phenyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: Silane, trimethyl[3-(trifluoromethyl)phenyl]-(4405-40-7)
• EPA Substance Registry System: Silane, trimethyl[3-(trifluoromethyl)phenyl]-(4405-40-7)

Safety Data

• Hazardous Substances Data: 4405-40-7(Hazardous Substances Data)

Upstream product

• 75-77-4 chloro-trimethyl-silane 
• 401-78-5 3-bromo-1-trifluoromethylbenzene 
• 98-15-7 3-chlorotrifluoromethylbenzene 
• 1450-14-2 1,1,1,2,2,2-hexamethyldisilane 
• 368-49-0 3-(trifluoromethyl)phenyllithium 

Downstream Products

• 196080-81-6 1-[difluoro(trimethylsilyl)methyl]-3-(trimethylsilyl)benzene 
• 196080-82-7 1-[fluoro-bis(trimethylsilyl)methyl]-3-(trimethylsilyl)benzene 
• 1355722-39-2 1-[fluoro-bis(trimethylsilyl)methyl]-4-(trimethylsilyl)benzene 
• 1449606-85-2 1-(2-methoxyethyl)-3-(trifluoromethyl)benzene 

Relevant articles and documents

Oxidative 1,2-Difunctionalization of Ethylene via Gold-Catalyzed Oxyarylation

Under the conditions of oxidative gold catalysis, exposure of ethylene to aryl silanes and alcohols generates products of 1,2-oxyarylation. This provides a rare example of a process that allows catalytic differential 1,2-difunctionalization of this feedstock chemical.

Cu-deposits on Mg metal surfaces promote electron transfer reactions

The enhancement of the electron transfer processes in the Grignard reagent formation-type ring silylation and the defluorination-silylation of perfluoroalkyl benzenes by Cu(0)-deposited Mg metal were confirmed. Microscopic analysis and substituent effects implied a different reduction process in the presence of Cu-deposited Mg metal than in the presence of bare Mg metal.