995-43-7

Basic information

• Product Name: Methyl-tri-n-butylsilane
• Synonyms: Methyl-tri-n-butylsilane
• CAS NO: 995-43-7
• Molecular Formula: C13H30Si
• Molecular Weight: 214.4628
• Mol File: 995-43-7.mol
• Article Data: 4

Chemical Properties

• Appearance: /
• CAS DataBase Reference: Methyl-tri-n-butylsilane(CAS DataBase Reference)
• NIST Chemistry Reference: Methyl-tri-n-butylsilane(995-43-7)
• EPA Substance Registry System: Methyl-tri-n-butylsilane(995-43-7)

Safety Data

• Hazardous Substances Data: 995-43-7(Hazardous Substances Data)

Usage

General Description

Methyl-tri-n-butylsilane is a chemical compound that consists of a methyl group and three n-butyl groups attached to a silicon atom. It is commonly used as a reagent in organic synthesis for the functionalization of silicon-based materials and as a cross-coupling agent in the formation of carbon-carbon bonds. Methyl-tri-n-butylsilane is a colorless liquid with a strong, unpleasant odor and is highly flammable. It is important to handle this chemical with caution and follow proper safety procedures when working with it.

Upstream product

• 693-03-8 n-butyl magnesium bromide 
• 75-79-6 Methyltrichlorosilane 
• 1116-70-7 tri(n-butyl)aluminium 
• 996-07-6 dibutyl-chloro-methyl-silane 
• 19284-22-1 n-butylmethylchlorosilane 
• 18143-64-1 butylmethylsilane 
• 18147-23-4 butyl-dichloro-methyl-silane 
• 106-98-9 1-butylene 
• 999-35-9 di-n-butylmethylsilane 
• 2031-67-6 Methyltriethoxysilan 
• 109-72-8 n-butyllithium 
• 1578-31-0 tri(2-furyl)methylsilane 
• 102129-44-2 sodium bis(1,2-benzenediolato)methylsilicate 

Relevant articles and documents

PROCESS FOR THE STEPWISE SYNTHESIS OF SILAHYDROCARBONS

The invention relates to a process for the stepwise synthesis of silahydrocarbons bearing up to four different organyl substituents at the silicon atom, wherein the process includes at least one step a) of producing a bifunctional hydridochlorosilane by a redistribution reaction, selective chlorination of hydridosilanes with an ether/HCI reagent, or by selective chlorination of hydridosilanes with SiCI4, at least one step b) of submitting a bifunctional hydridochloromonosilane to a hydrosilylation reaction, at least one step c) of hydrogenation of a chloromonosilane, and a step d) in which a silahydrocarbon compound is obtained in a hydrosilylation reaction.

Reactivity of Hypervalent Species: Reactions of Anionic Penta-Coordinated Silicon Complexes towards Nucleophiles

The reactivity of anionic penta-coordinated silicon complexes 4-O)2>-Na+ 1 with nucleophilic reagents has been studied. 1 can be reduced to organosilanes RSiH3 by metallic hydrides.Reactions with an excess of Grignard or organolithium reagents (R'MgX or R'Li) gave tetraorganosilanes RSiR'3.When only two molar equivalents of Grignard reagents (R'MgX) or lithium reagents (R'Li) are added to complexs 1 functional silanes RR'2SiX can be prepared.