Bis(1-phenylethyl) selenide

Base Information

Chemical Name:Bis(1-phenylethyl) selenide
CAS No.:116747-64-9
Molecular Formula:C16H18Se
Molecular Weight:289.279
Hs Code.:
DSSTox Substance ID:DTXSID201287186
Nikkaji Number:J992.182F
Mol file:116747-64-9.mol

Synonyms:Bis(1-phenylethyl) selenide;DTXSID201287186;1,1'-(Selenodiethylidene)bis[benzene];116747-64-9

Suppliers and Price of Bis(1-phenylethyl) selenide

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

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Chemical Property of Bis(1-phenylethyl) selenide

Chemical Property:

Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:0
Rotatable Bond Count:4
Exact Mass:290.05737
Heavy Atom Count:17
Complexity:180

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC(C1=CC=CC=C1)[Se]C(C)C2=CC=CC=C2

Technology Process of Bis(1-phenylethyl) selenide

There total 2 articles about Bis(1-phenylethyl) selenide 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: 98.0%

: 585-71-7,38661-81-3
(1-bromoethyl)benzne

: 116747-64-9
bis(1-phenylethyl) selenide

Guidance literature:: With selenium; sodium tetrahydroborate; ethanol; In N,N-dimethyl-formamide; at 20 ℃;
DOI:10.1055/s-2004-829554

Reference yield: 55.0%

: 100-42-5,25038-60-2,25247-68-1,28213-80-1,28325-75-9,79637-11-9,9003-53-6
styrene

: 585-71-7,38661-81-3
(1-bromoethyl)benzne

: 116747-64-9
bis(1-phenylethyl) selenide

Guidance literature:: (1-bromoethyl)benzne; With magnesium; In tetrahydrofuran; at 45 ℃; for 1h; Inert atmosphere;

With selenium; In tetrahydrofuran; for 0.5h; Inert atmosphere;

styrene; With copper(l) iodide; L-proline; In tetrahydrofuran; water; toluene; at 85 ℃; for 8h; regioselective reaction; Inert atmosphere;
DOI:10.1016/j.tetlet.2012.08.046