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(E)-1-Trimethylsilyl-1,3-butadiene

Base Information
  • Chemical Name:(E)-1-Trimethylsilyl-1,3-butadiene
  • CAS No.:71504-26-2
  • Molecular Formula:C7H14Si
  • Molecular Weight:126.274
  • Hs Code.:
  • DSSTox Substance ID:DTXSID80437097
(E)-1-Trimethylsilyl-1,3-butadiene

Synonyms:71504-26-2;(E)-1-TRIMETHYLSILYL-1,3-BUTADIENE;1-trimethylsilylbutadiene;DTXSID80437097

Suppliers and Price of (E)-1-Trimethylsilyl-1,3-butadiene
Supply Marketing:
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 1 raw suppliers
Chemical Property of (E)-1-Trimethylsilyl-1,3-butadiene
Chemical Property:
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:0
  • Rotatable Bond Count:2
  • Exact Mass:126.086476981
  • Heavy Atom Count:8
  • Complexity:95.4
Purity/Quality:

99% *data from raw suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:C[Si](C)(C)C=CC=C
  • Physical properties bp 110–115 °C, 70–74 °C/210 mmHg.
  • Uses As as useful reagent, (E)-1-Trimethylsilyl-1,3-butadiene is used as a diene for Diels–Alder reactions, creating allylsilanes that can be converted to a variety of functionalized cyclohexenes with a shift of the double bond from its original position in the cycloaddition; synthesis of a chiral allylborane; synthesis of allylsilanes and trienes
Technology Process of (E)-1-Trimethylsilyl-1,3-butadiene

There total 5 articles about (E)-1-Trimethylsilyl-1,3-butadiene 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 toluene-4-sulfonic acid; In diethyl ether; for 1h; Yield given. Yields of byproduct given. Title compound not separated from byproducts; Ambient temperature;
DOI:10.1039/P19810002415
Guidance literature:
In tetrahydrofuran; for 1h; Yield given. Title compound not separated from byproducts; Ambient temperature;
DOI:10.1039/P19810002415
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