{[(2-Methylpropane-2-sulfonyl)methyl]selanyl}benzene

Base Information

Chemical Name:{[(2-Methylpropane-2-sulfonyl)methyl]selanyl}benzene
CAS No.:141341-43-7
Molecular Formula:C11H16O2SSe
Molecular Weight:291.273
Hs Code.:
DSSTox Substance ID:DTXSID60579863
Wikidata:Q82470500
Mol file:141341-43-7.mol

Synonyms:141341-43-7;{[(2-Methylpropane-2-sulfonyl)methyl]selanyl}benzene;DTXSID60579863

Suppliers and Price of {[(2-Methylpropane-2-sulfonyl)methyl]selanyl}benzene

Supply Marketing:

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

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Chemical Property of {[(2-Methylpropane-2-sulfonyl)methyl]selanyl}benzene

Chemical Property:

Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:4
Exact Mass:292.00362
Heavy Atom Count:15
Complexity:279

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

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

Technology Process of {[(2-Methylpropane-2-sulfonyl)methyl]selanyl}benzene

There total 2 articles about {[(2-Methylpropane-2-sulfonyl)methyl]selanyl}benzene 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: 89.0%

: 5707-04-0
Phenylselenyl chloride

: 14094-12-3
tert-butyl methyl sulfone

: 141341-43-7
tert-butyl (phenylselenyl)methyl sulfone

Guidance literature:: With lithium diisopropyl amide; In tetrahydrofuran; for 2h; Ambient temperature;
DOI:10.1002/hlca.19930760707

Reference yield:

: 6163-64-0
tert-butyl methyl sulphide

: 141341-43-7
tert-butyl (phenylselenyl)methyl sulfone

Guidance literature:: Multi-step reaction with 2 steps

1: 51 percent / Oxone (48percent) / H₂O; methanol / 12 h / Ambient temperature

2: 89 percent / LDA / tetrahydrofuran / 2 h / Ambient temperature

With Oxone; lithium diisopropyl amide; In tetrahydrofuran; methanol; water;
DOI:10.1002/hlca.19930760707