3-Methyl-5-(2-phenylethyl)-5H-1,4,2-oxathiazole

Base Information

Chemical Name:3-Methyl-5-(2-phenylethyl)-5H-1,4,2-oxathiazole
CAS No.:88358-61-6
Molecular Formula:C11H13NOS
Molecular Weight:207.296
Hs Code.:
DSSTox Substance ID:DTXSID60530535

Synonyms:88358-61-6;3-Methyl-5-(2-phenylethyl)-5H-1,4,2-oxathiazole;DTXSID60530535

Suppliers and Price of 3-Methyl-5-(2-phenylethyl)-5H-1,4,2-oxathiazole

Supply Marketing:

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

Manufacturers and distributors:

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Total 0 raw suppliers

Chemical Property of 3-Methyl-5-(2-phenylethyl)-5H-1,4,2-oxathiazole

Chemical Property:

XLogP3:3.3
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:3
Exact Mass:207.07178521
Heavy Atom Count:14
Complexity:211

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1=NOC(S1)CCC2=CC=CC=C2

Technology Process of 3-Methyl-5-(2-phenylethyl)-5H-1,4,2-oxathiazole

There total 2 articles about 3-Methyl-5-(2-phenylethyl)-5H-1,4,2-oxathiazole 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:

: 88358-54-7
2-(tert-Butyl-dimethyl-silanyloxy)-3-methyl-5-phenethyl-[1,4,2]oxathiazolidine

: 104-53-0
3-phenyl-propionaldehyde

: 88358-61-6
3-Methyl-5-phenethyl-[1,4,2]oxathiazole

Guidance literature:: With hydrogenchloride; In tetrahydrofuran;
DOI:10.1021/jo00177a045

Reference yield:

: 87598-28-5
1-Phenyl-2-(3-phenyl-propylsulfanyl)-ethanone

: 88358-61-6
3-Methyl-5-phenethyl-[1,4,2]oxathiazole

Guidance literature:: Multi-step reaction with 2 steps

1: 91 percent / benzene / 2 h / Ambient temperature; Irradiation

2: HCl / tetrahydrofuran

With hydrogenchloride; In tetrahydrofuran; benzene;
DOI:10.1021/jo00177a045