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2,5-Diphenylselenophene

Base Information Edit
  • Chemical Name:2,5-Diphenylselenophene
  • CAS No.:18782-55-3
  • Molecular Formula:C16H12Se
  • Molecular Weight:283.231
  • Hs Code.:
  • DSSTox Substance ID:DTXSID30399191
  • Nikkaji Number:J961.058H
  • Wikidata:Q82201587
  • Mol file:18782-55-3.mol
2,5-Diphenylselenophene

Synonyms:2,5-diphenylselenophene;18782-55-3;AI-942/25034926;YSCK0320;DTXSID30399191

Suppliers and Price of 2,5-Diphenylselenophene
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 2,5-Diphenylselenophene Edit
Chemical Property:
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:0
  • Rotatable Bond Count:2
  • Exact Mass:284.01042
  • Heavy Atom Count:17
  • Complexity:202
Purity/Quality:

99% *data from raw suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:C1=CC=C(C=C1)C2=CC=C([Se]2)C3=CC=CC=C3
Technology Process of 2,5-Diphenylselenophene

There total 24 articles about 2,5-Diphenylselenophene 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 woollins’ reagent; In toluene; for 20h; Inert atmosphere; Reflux;
DOI:10.1039/b924986a
Guidance literature:
2,5-diphenyl-3-iodoselenophene; With n-butyllithium; In hexane; at -78 - 20 ℃;
With water; In hexane; for 0.166667h; Further stages.;
DOI:10.1021/jo070835t
Guidance literature:
With selenium; 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical; potassium hydroxide; In dimethyl sulfoxide; at 80 ℃; for 4h; Solvent; Reagent/catalyst; Catalytic behavior; Schlenk technique; Inert atmosphere;
DOI:10.1021/acs.joc.1c00874
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