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Diselenide, bis[2,4,6-tris(1-methylethyl)phenyl]

Base Information
  • Chemical Name:Diselenide, bis[2,4,6-tris(1-methylethyl)phenyl]
  • CAS No.:71518-96-2
  • Molecular Formula:C30H46Se2
  • Molecular Weight:564.615
  • Hs Code.:
  • DSSTox Substance ID:DTXSID70471900
  • Nikkaji Number:J1.071.719A
  • Wikidata:Q82300595
Diselenide, bis[2,4,6-tris(1-methylethyl)phenyl]

Synonyms:Diselenide, bis[2,4,6-tris(1-methylethyl)phenyl];71518-96-2;DTXSID70471900;di(2,4,6-triisopropylphenyl)diselenide

Suppliers and Price of Diselenide, bis[2,4,6-tris(1-methylethyl)phenyl]
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
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Total 0 raw suppliers
Chemical Property of Diselenide, bis[2,4,6-tris(1-methylethyl)phenyl]
Chemical Property:
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:0
  • Rotatable Bond Count:9
  • Exact Mass:566.19299
  • Heavy Atom Count:32
  • Complexity:451
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CC(C)C1=CC(=C(C(=C1)C(C)C)[Se][Se]C2=C(C=C(C=C2C(C)C)C(C)C)C(C)C)C(C)C
Technology Process of Diselenide, bis[2,4,6-tris(1-methylethyl)phenyl]

There total 4 articles about Diselenide, bis[2,4,6-tris(1-methylethyl)phenyl] 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:
2,4,6-triisopropyl-1-bromobenzene; With tert.-butyl lithium; at -78 ℃;
With selenium; at -78 - 20 ℃;
With ammonium chloride; at 20 ℃;
DOI:10.1016/j.tetlet.2005.05.052
Guidance literature:
In not given; byproducts: I2; inert solvents; equilibrium mixt. monitored by UV and NMR;
Guidance literature:
With tetraethylammonium iodide;
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