Stannane, tributyl(2-phenylethenyl)-, (E)-

Base Information Edit

Chemical Name:Stannane, tributyl(2-phenylethenyl)-, (E)-
CAS No.:66680-88-4
Molecular Formula:C₂₀H₃₄Sn
Molecular Weight:393.2
Hs Code.:
Mol file:66680-88-4.mol

Synonyms:

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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 Stannane, tributyl(2-phenylethenyl)-, (E)- Edit

Chemical Property:

PSA：0.00000
LogP:7.08810

Purity/Quality:

Safty Information:

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Hazard Codes:

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Technology Process of Stannane, tributyl(2-phenylethenyl)-, (E)-

There total 27 articles about Stannane, tributyl(2-phenylethenyl)-, (E)- 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: 100.0%

: 688-73-3
tri-n-butyl-tin hydride

: 536-74-3
phenylacetylene

: 66680-87-3,66680-88-4,79159-76-5
(E)-1-phenyl-(2-tributylstannyl)ethene

Guidance literature:: With 2,2'-azobis(isobutyronitrile); oxygen; In benzene-d6; at 80 ℃; for 2h; diastereoselective reaction;
DOI:10.1002/anie.201303736

Reference yield: 98.0%

: 688-73-3
tri-n-butyl-tin hydride

: C₃₆H₄₇FeOP

: 66680-87-3,66680-88-4,79159-76-5
(E)-1-phenyl-(2-tributylstannyl)ethene

: Cp*Fe(1,2-PCy₂C₆H₄O)

Guidance literature:: In toluene; at 20 ℃; Inert atmosphere;
DOI:10.1021/jacs.0c11448

Reference yield: 97.0%

: 688-73-3
tri-n-butyl-tin hydride

: Cp*Fe(1,2-PCy₂C₆H₄O)

: 536-74-3
phenylacetylene

: 66680-87-3,66680-88-4,79159-76-5
(E)-1-phenyl-(2-tributylstannyl)ethene

Guidance literature:: Cp*Fe(1,2-PCy₂C₆H₄O); phenylacetylene; In toluene; at 20 ℃; for 0.0833333h; Inert atmosphere;

tri-n-butyl-tin hydride; In toluene; at 20 ℃; for 12h; Reagent/catalyst; regioselective reaction; Inert atmosphere;
DOI:10.1021/jacs.0c11448