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1,2-Bis(2,4,6-trimethylphenyl)disilane

Base Information Edit
  • Chemical Name:1,2-Bis(2,4,6-trimethylphenyl)disilane
  • CAS No.:139039-99-9
  • Molecular Formula:C18H26Si2
  • Molecular Weight:298.575
  • Hs Code.:
  • DSSTox Substance ID:DTXSID40769386
  • Mol file:139039-99-9.mol
1,2-Bis(2,4,6-trimethylphenyl)disilane

Synonyms:1,2-Bis(2,4,6-trimethylphenyl)disilane;139039-99-9;DTXSID40769386

Suppliers and Price of 1,2-Bis(2,4,6-trimethylphenyl)disilane
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 1 raw suppliers
Chemical Property of 1,2-Bis(2,4,6-trimethylphenyl)disilane Edit
Chemical Property:
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:0
  • Rotatable Bond Count:3
  • Exact Mass:294.12600377
  • Heavy Atom Count:20
  • Complexity:250
Purity/Quality:

99.90% *data from raw suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:CC1=CC(=C(C(=C1)C)[Si][Si]C2=C(C=C(C=C2C)C)C)C
Technology Process of 1,2-Bis(2,4,6-trimethylphenyl)disilane

There total 4 articles about 1,2-Bis(2,4,6-trimethylphenyl)disilane 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 lithium; In diethyl ether; at 20 ℃; for 48h;
Guidance literature:
With 1,2-bis(trifluoromethanesulfonyloxy)disilane; In tetrahydrofuran; toluene; at -50 - 20 ℃;
Guidance literature:
With C24H45ClIrNO2P2; at 120 ℃; for 16h; Inert atmosphere;
DOI:10.1021/acs.organomet.5b00486
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