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(Dibromomethyl)trimethylsilane

Base Information Edit
  • Chemical Name:(Dibromomethyl)trimethylsilane
  • CAS No.:2612-42-2
  • Molecular Formula:C4H10Br2Si
  • Molecular Weight:246.017
  • Hs Code.:2931900090
  • Mol file:2612-42-2.mol
(Dibromomethyl)trimethylsilane

Synonyms:(Dibromomethyl)trimethylsilane;Dibromo(trimethylsilyl)methane

Suppliers and Price of (Dibromomethyl)trimethylsilane
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
Total 5 raw suppliers
Chemical Property of (Dibromomethyl)trimethylsilane Edit
Chemical Property:
  • Boiling Point:82.5 °C(Press: 50 Torr) 
  • PSA:0.00000 
  • Density:1.566±0.06 g/cm3(Predicted) 
  • LogP:3.39960 
  • Solubility.:sol most organic solvents. 
Purity/Quality:

99% *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Physical properties bp 49.5–51.5°C/12 mmHg; d 1.519 g cm?3.
  • Uses Reaction of (dibromomethyl)- trimethylsilane with n-butyllithium at ?110°C results in the formation of trimethylsilylbromomethyllithium. The silane and the n-BuLi are added simultaneously in order to suppress side reactions. Treatment of the intermediate lithium reagent with chlorotrimethylsilane (eq 1) or mercury(II) bromide (eq 2) affords bis(trimethylsilyl)bromomethane or bis(trimethylsilylbromomethyl) mercury, respectively. If the lithium reagent is allowed to warm in the presence of cyclohexene, the only reaction observed is an alkylation with the n-butyl bromide formed in the exchange reaction. The alkylated product is formed in 89% yield.
Technology Process of (Dibromomethyl)trimethylsilane

There total 6 articles about (Dibromomethyl)trimethylsilane which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
With n-butyllithium; In tetrahydrofuran; hexane; at -78 ℃; Yields of byproduct given;
Guidance literature:
Multistep reaction; (i) LDA, (ii) /BRN= 1209232/;
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