2,5-Diphenylselenophene

Base Information

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

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

Suppliers and Price of 2,5-Diphenylselenophene

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 2,5-Diphenylselenophene

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:

Reference yield: 99.0%

: 495-71-6
phenacylacetophenone

: 18782-55-3
2,5-bis-phenylselenophene

Guidance literature:: With woollins’ reagent; In toluene; for 20h; Inert atmosphere; Reflux;
DOI:10.1039/b924986a

Reference yield: 97.0%

: 950894-38-9
2,5-diphenyl-3-iodoselenophene

: 18782-55-3
2,5-bis-phenylselenophene

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

Reference yield: 85.0%

: 886-66-8
1,4-diphenyl-1,3-butadiyne

: 18782-55-3
2,5-bis-phenylselenophene

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