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Ethanone, 2-[(4-methylphenyl)sulfonyl]-2-(methylthio)-1-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

87228-53-3

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87228-53-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 87228-53-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,2,2 and 8 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 87228-53:
(7*8)+(6*7)+(5*2)+(4*2)+(3*8)+(2*5)+(1*3)=153
153 % 10 = 3
So 87228-53-3 is a valid CAS Registry Number.

87228-53-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(4-methylphenyl)sulfonyl-2-methylsulfanyl-1-phenylethanone

1.2 Other means of identification

Product number -
Other names Ethanone,2-[(4-methylphenyl)sulfonyl]-2-(methylthio)-1-phenyl

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:87228-53-3 SDS

87228-53-3Relevant academic research and scientific papers

Direct and Efficient Synthesis of Sulfonium Acyl Sulfonylmethylide Ylides from Acetylenic Sulfones and Dimethyl Sulfoxide

Fu, Duo,Wang, Jiayi,Xu, Jiaxi

, p. 4086 - 4096 (2021/08/10)

Bifunctionalized sulfonium ylides - sulfonium acyl sulfonylmethylides - were directly and efficiently prepared from various acetylenic sulfones and aliphatic sulfoxides under heating conditions. The current method features short reaction time, low cost, readily available starting materials, convenient operation, and purification, providing an efficient access to widely applied bifunctionalized sulfonium ylides.

A VERSATILE REAGENT FOR SYNTHESIS OF α-HYDROXY ALDEHYDES AND KETONES --- METHYLTHIOMETHYL p-TOLYL SULFONE

Ogura, Katsuyuki,Tsuruda, Toshihiko,Takahashi, Kazumasa,Iida, Hirotada

, p. 3665 - 3668 (2007/10/02)

Methylthiomethyl p-tolyl sulfone (1) can be utilized for synthesizing α-hydroxy ketones as well as α-hydroxy aldehydes, the hydroxyl group of which is protected with acetyl, tetrahydropyranyl, or methoxymethyl group.

UTILIZATION OF METHYLTHIOMETHYL p-TOLYL SULFONE IN ORGANIC SYNTHESIS

Ogura, Katsuyuki,Yahata, Nobuhiro,Hashizume, Kimitoshi,Tsuyama, Koichi,Takahashi, Kazumasa,Iida, Hirotada

, p. 767 - 770 (2007/10/02)

Methylthiomethyl p-tolyl sulfone was found to be one of the useful reagents for preparation of various organic compounds such as S-methyl α-ketocarbothioates, carboxylic esters, five- and six-membered cycloalkanones, and α-methoxy-α-arylacetic esters.

A NOVEL ROUTE FROM A CARBOXYLIC ACID TO A CARBALDEHYDE USING METHYLTHIOMETHYL p-TOLYL SULFONE

Ogura, Katsuyuki,Yahata, Nobuhiro,Takahashi, Kazumasa,Iida, Hirotada

, p. 5761 - 5762 (2007/10/02)

A new conversion of a carboxylic ester to a carbaldehyde involing formation and dissociation of a C-C bond at the acyl carbon was accomplished by the use of methylthiomethyl p-tolyl sulfone (1).

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