1-[Dimethyl(phenyl)silyl]butyl selenocyanate

Base Information

Chemical Name:1-[Dimethyl(phenyl)silyl]butyl selenocyanate
CAS No.:100604-91-9
Molecular Formula:C13H19NSeSi
Molecular Weight:296.346
Hs Code.:
DSSTox Substance ID:DTXSID00544353
Mol file:100604-91-9.mol

Synonyms:100604-91-9;1-[Dimethyl(phenyl)silyl]butyl selenocyanate;Selenocyanic acid, 1-(dimethylphenylsilyl)butyl ester;DTXSID00544353

Suppliers and Price of 1-[Dimethyl(phenyl)silyl]butyl selenocyanate

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 1-[Dimethyl(phenyl)silyl]butyl selenocyanate

Chemical Property:

Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:5
Exact Mass:297.04520
Heavy Atom Count:16
Complexity:250

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

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

Technology Process of 1-[Dimethyl(phenyl)silyl]butyl selenocyanate

There total 2 articles about 1-[Dimethyl(phenyl)silyl]butyl selenocyanate 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: 91.0%

: 3425-46-5
potassium selenocyanate

: 100604-84-0
1-(dimethylphenylsilyl)butyl p-toluenesulfonate

: 100604-91-9
1-(dimethylphenylsilyl)butyl selenocyanate

Guidance literature:: With 18-crown-6 ether; In tetrahydrofuran; Heating;
DOI:10.1021/ja00234a015

Reference yield:

: 3839-31-4
dimethyl(phenyl)silyllithium

: 100604-91-9
1-(dimethylphenylsilyl)butyl selenocyanate

Guidance literature:: Multi-step reaction with 2 steps

1: tetrahydrofuran / -78 °C

2: 18-C-6 / tetrahydrofuran

With 18-crown-6 ether; In tetrahydrofuran;
DOI:10.1021/ja00266a041