Diselenide, bis[(2-fluorophenyl)methyl]

Base Information

Chemical Name:Diselenide, bis[(2-fluorophenyl)methyl]
CAS No.:823178-70-7
Molecular Formula:C14H12F2Se2
Molecular Weight:376.166
Hs Code.:
DSSTox Substance ID:DTXSID00465635
Wikidata:Q82291763

Synonyms:Diselenide, bis[(2-fluorophenyl)methyl];823178-70-7;DTXSID00465635

Suppliers and Price of Diselenide, bis[(2-fluorophenyl)methyl]

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 Diselenide, bis[(2-fluorophenyl)methyl]

Chemical Property:

Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:5
Exact Mass:377.92375
Heavy Atom Count:18
Complexity:214

Purity/Quality:: 85.0-99.8% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C(=C1)C[Se][Se]CC2=CC=CC=C2F)F

Technology Process of Diselenide, bis[(2-fluorophenyl)methyl]

There total 4 articles about Diselenide, bis[(2-fluorophenyl)methyl] 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: 85.0%

: 1-(2-fluorophenyl)-N,N,N-trimethylmethanammonium triflate

: 823178-70-7
1,2-bis(2-fluorobenzyl)diselane

Guidance literature:: With selenium; caesium carbonate; In acetonitrile; at 80 ℃; for 16h; Inert atmosphere; Sealed tube;
DOI:10.1002/ejoc.202101086

Reference yield:

: 446-48-0
o-fluorobenzyl bromide

: 823178-70-7
1,2-bis(2-fluorobenzyl)diselane

Guidance literature:: Multi-step reaction with 2 steps

1: 63 percent / ethanol / 0.17 h

2: 1.52 g / sodium hydroxide / ethanol; H₂O / 1 h

With sodium hydroxide; In ethanol; water;
DOI:10.1021/jo048436a