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Sulfoximine, S-methyl-S-phenyl-N-(phenylsulfonyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

80816-44-0

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80816-44-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 80816-44-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,8,1 and 6 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 80816-44:
(7*8)+(6*0)+(5*8)+(4*1)+(3*6)+(2*4)+(1*4)=130
130 % 10 = 0
So 80816-44-0 is a valid CAS Registry Number.

80816-44-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(methyl-oxo-phenyl-λ<sup>6</sup>-sulfanylidene)benzenesulfonamide

1.2 Other means of identification

Product number -
Other names HMS1577D16

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:80816-44-0 SDS

80816-44-0Downstream Products

80816-44-0Relevant academic research and scientific papers

I2-Catalyzed N-Sulfonylation of Sulfoximines with Sulfinates in Water at Room Temperature

Zheng, Wenting,Tan, Mingchao,Yang, Lu,Zhou, Lihong,Zeng, Qingle

, p. 1764 - 1768 (2020/03/13)

An oxidative coupling of NH-sulfoximines and arylsulfinates catalyzed by of I2 and H2O2 affords N-sulfonyl sulfoximines. The reaction proceeds under aerobic conditions in water at room temperature. The merits of this proto

Synthetic method of N-aryl sulfone sulfoximine

-

Paragraph 0009-0013, (2019/12/25)

Sulfoximines have a wide range of applications in organic chemistry, medicinal chemistry, agricultural chemistry, sulfimides are related to the medicinal activity of various organisms, such as antiarrhythmic, antispasmodic, antiasthmatic and antiviral act

Copper-catalyzed imination of sulfoxides and sulfides

Liu, Yuanyuan,Wang, Hanying,Yang, Xianjin

supporting information, p. 4697 - 4702 (2019/07/22)

Sulfoximines and sulfilimines have attracted considerable interest among organic chemists. The Cu(II)-catalyzed imination of sulfoxides and sulfides using various N-fluoro benzenesulfonamides was investigated in this study. The scope of the reaction was demonstrated by using several substituted sulfides and sulfoxides. The flow strategy for the preparation of NH-sulfoximines was also examined. By trapping nitrene intermediates through triphenylphosphine, we found that the reaction was conducted through a metal-nitrene intermediate mechanism.

A CONVENIENT PREPARATION OF N-(ARENESULFONYL)SULFOXIMINES BY OXIDATION OF N-(ARENESULFONYL)SULFILIMINES WITH SODIUM HYPOCHLORITE IN A TWO PHASE SYSTEM

Furukawa, Naomichi,Akutagawa, Kunihiko,Yoshimura, Toshiaki,Oae, Shigeru

, p. 3989 - 3992 (2007/10/02)

N-(Arenesulfonyl)sulfilimines can be oxidized to the corresponding sulfoximines in high yields with sodium hypochlorite in an AcOEt-H2O two phase system in the presence of quaternary ammonium salts as catalysts.

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