Silane, trimethyl[1-(phenylseleno)ethenyl]-

Base Information

Chemical Name:Silane, trimethyl[1-(phenylseleno)ethenyl]-
CAS No.:77461-49-5
Molecular Formula:C11H16SeSi
Molecular Weight:255.294
Hs Code.:
DSSTox Substance ID:DTXSID70446532
Nikkaji Number:J496.119F
Wikidata:Q82265206

Synonyms:Silane, trimethyl[1-(phenylseleno)ethenyl]-;77461-49-5;DTXSID70446532;1-Trimethylsilyl-1-(phenylseleno)ethene

Suppliers and Price of Silane, trimethyl[1-(phenylseleno)ethenyl]-

Supply Marketing:

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

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Chemical Property of Silane, trimethyl[1-(phenylseleno)ethenyl]-

Chemical Property:

Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:0
Rotatable Bond Count:3
Exact Mass:256.01865
Heavy Atom Count:13
Complexity:175

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

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

Technology Process of Silane, trimethyl[1-(phenylseleno)ethenyl]-

There total 4 articles about Silane, trimethyl[1-(phenylseleno)ethenyl]- 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:

: 1666-13-3
diphenyl diselenide

: 77461-49-5
1-(Phenylseleno)-1-(trimethylsilyl)ethene

Guidance literature:: Multi-step reaction with 2 steps

1: Br₂ / tetrahydrofuran

2: 1) Mg, 1,2-dibromoethane / 1) THF, reflux, 1 h, 2) THF, reflux, 1 h

With bromine; magnesium; ethylene dibromide; In tetrahydrofuran;

Reference yield:

: 34837-55-3
Phenylselenyl bromide

: 77461-49-5
1-(Phenylseleno)-1-(trimethylsilyl)ethene

Guidance literature:: Multi-step reaction with 2 steps

1: 1.) Mg / 1.) THF, reflux, 20 min, 2.) 45 min

2: 1.) LDA / 1.) THF, hexane, -78 deg C, 2 h, 2.) -78 deg C, 15 min

With magnesium; lithium diisopropyl amide;
DOI:10.1021/jo00326a035

Reference yield:

: 75-77-4
chloro-trimethyl-silane

: 35167-28-3
vinyl phenyl selenide

: 77461-49-5
1-(Phenylseleno)-1-(trimethylsilyl)ethene

Guidance literature:: With lithium diisopropyl amide; Yield given. Multistep reaction; 1.) THF, hexane, -78 deg C, 2 h, 2.) -78 deg C, 15 min;
DOI:10.1021/jo00326a035