Disulfide, 1,1-dimethylethyl phenylmethyl

Base Information

Chemical Name:Disulfide, 1,1-dimethylethyl phenylmethyl
CAS No.:33663-80-8
Molecular Formula:C11H16S2
Molecular Weight:212.38
Hs Code.:
DSSTox Substance ID:DTXSID90449666
Nikkaji Number:J448.258A
Wikidata:Q82269189

Synonyms:33663-80-8;Disulfide, 1,1-dimethylethyl phenylmethyl;Benzyl tert-butyl persulfide;DTXSID90449666

Suppliers and Price of Disulfide, 1,1-dimethylethyl phenylmethyl

Supply Marketing:

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

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Chemical Property of Disulfide, 1,1-dimethylethyl phenylmethyl

Chemical Property:

XLogP3:3.4
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:4
Exact Mass:212.06934286
Heavy Atom Count:13
Complexity:132

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(C)(C)SSCC1=CC=CC=C1

Technology Process of Disulfide, 1,1-dimethylethyl phenylmethyl

There total 12 articles about Disulfide, 1,1-dimethylethyl phenylmethyl 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: 80.0%

: 100-39-0
benzyl bromide

: 1-(tert-butyldisulfanyl)pentan-3-one

: 33663-80-8
1-benzyl-2-(tert-butyl)disulfane

Guidance literature:: With caesium carbonate; In methanol; at 30 ℃; for 14h; Inert atmosphere;

Reference yield: 74.0%

: 75-66-1
2-methylpropan-2-thiol

: 100-53-8
phenylmethanethiol

: 33663-80-8
1-benzyl-2-(tert-butyl)disulfane

Guidance literature:: tetra(n-butyl)ammonium hydroxide; In benzene; for 36h; Ambient temperature; other thiols, var. catalyst, var. time;
DOI:10.1246/bcsj.65.626