bis-(phenyl ethynyl)selenide

Base Information

Chemical Name:bis-(phenyl ethynyl)selenide
CAS No.:120880-80-0
Molecular Formula:C₁₆H₁₀Se
Molecular Weight:281.215
Hs Code.:

Synonyms:bis-(phenyl ethynyl)selenide

Suppliers and Price of bis-(phenyl ethynyl)selenide

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

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Chemical Property of bis-(phenyl ethynyl)selenide

Chemical Property:

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Technology Process of bis-(phenyl ethynyl)selenide

There total 6 articles about bis-(phenyl ethynyl)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: 90.0%

: C₄₀H₃₂O₈P₂Se

: 120880-80-0
bis-(phenyl ethynyl)selenide

Guidance literature:: With lithium hexamethyldisilazane; In tetrahydrofuran; ethylbenzene; at -78 ℃; Inert atmosphere;
DOI:10.1002/hc.21208

Reference yield: 87.0%

: 39167-49-2
1,5-diphenyl-3-selena-1,5-pentanedione

: 120880-80-0
bis-(phenyl ethynyl)selenide

Guidance literature:: 1,5-diphenyl-3-selena-1,5-pentanedione; With lithium hexamethyldisilazane; In tetrahydrofuran; ethylbenzene; at -78 ℃; for 0.5h; Inert atmosphere;

With chlorophosphoric acid diphenyl ester; In tetrahydrofuran; ethylbenzene; at -78 - 20 ℃; for 1.5h; Inert atmosphere;

With lithium hexamethyldisilazane; In tetrahydrofuran; ethylbenzene; at -78 ℃; for 1h; Reagent/catalyst; Inert atmosphere;
DOI:10.1002/hc.21208

Reference yield: 85.0%

: 536-74-3
phenylacetylene

: 120880-80-0
bis-(phenyl ethynyl)selenide

Guidance literature:: With selenium; silver fluoride; In dimethyl sulfoxide; at 50 ℃; for 10h; Reagent/catalyst; Solvent; Time; chemoselective reaction;
DOI:10.1016/j.tet.2020.131083