Sulfoximine, S-methyl-S-phenyl-N-(phenylmethyl)-

Base Information

Chemical Name:Sulfoximine, S-methyl-S-phenyl-N-(phenylmethyl)-
CAS No.:37754-85-1
Molecular Formula:C14H15NOS
Molecular Weight:245.345
Hs Code.:
DSSTox Substance ID:DTXSID90401820
Nikkaji Number:J531.193D

Synonyms:Sulfoximine, S-methyl-S-phenyl-N-(phenylmethyl)-;37754-85-1;DTXSID90401820;N-Benzyl-S-methyl-S-phenylsulfoximine

Suppliers and Price of Sulfoximine, S-methyl-S-phenyl-N-(phenylmethyl)-

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 Sulfoximine, S-methyl-S-phenyl-N-(phenylmethyl)-

Chemical Property:

XLogP3:3.5
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:3
Exact Mass:245.08743528
Heavy Atom Count:17
Complexity:332

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CS(=NCC1=CC=CC=C1)(=O)C2=CC=CC=C2

Technology Process of Sulfoximine, S-methyl-S-phenyl-N-(phenylmethyl)-

There total 4 articles about Sulfoximine, S-methyl-S-phenyl-N-(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: 90.0%

: 100-39-0
benzyl bromide

: 4381-25-3
S-methyl-S-phenylsulfoximine

: 37754-85-1
(N-Benzyl)-methylphenylsulfoximid

Guidance literature:: With tetrabutylammomium bromide; potassium hydride; In 1,2-dimethoxyethane; at 20 ℃; for 1h;
DOI:10.1002/ejoc.200901462

Reference yield:

: (±)-N-benzylmethanesulfinamide

: 37754-85-1
(N-Benzyl)-methylphenylsulfoximid

Guidance literature:: Multi-step reaction with 2 steps

1: iodosylbenzene / 0.25 h / 20 °C

2: tetrahydrofuran / 0.75 h / -78 - 20 °C

With iodosylbenzene; In tetrahydrofuran;
DOI:10.1021/acs.orglett.8b01473