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2-(METHYLSULFONYL)-1-[3-(TRIFLUOROMETHYL)PHENYL]ETHANONE is a chemical compound characterized by the molecular formula C11H11F3O3S. It is a ketone derivative featuring a trifluoromethylphenyl group attached to the carbon chain and a methylsulfonyl group at the alpha carbon. 2-(METHYLSULFONYL)-1-[3-(TRIFLUOROMETHYL)PHENYL]ETHANONE is known for its versatile chemical properties and potential applications in various fields.

128306-96-7

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128306-96-7 Usage

Uses

Used in Pharmaceutical Industry:
2-(METHYLSULFONYL)-1-[3-(TRIFLUOROMETHYL)PHENYL]ETHANONE is used as an intermediate in the synthesis of pharmaceutical drugs. Its unique structure and functional groups make it a valuable building block for the development of new medications with improved efficacy and selectivity.
Used in Agrochemical Industry:
In the agrochemical sector, 2-(METHYLSULFONYL)-1-[3-(TRIFLUOROMETHYL)PHENYL]ETHANONE serves as an intermediate for the synthesis of agrochemicals. Its incorporation into these products can enhance their performance and selectivity, leading to more effective pest control and crop protection.
Used in Organic Synthesis:
2-(METHYLSULFONYL)-1-[3-(TRIFLUOROMETHYL)PHENYL]ETHANONE is utilized as a building block in organic synthesis, particularly in the preparation of heterocyclic compounds. Its presence in these reactions can facilitate the formation of complex molecular structures with potential applications in various industries.
Used in Material Production for Pharmaceutical and Agrochemical Applications:
2-(METHYLSULFONYL)-1-[3-(TRIFLUOROMETHYL)PHENYL]ETHANONE also shows promise as a building block in the production of materials for pharmaceutical and agrochemical applications. Its unique properties can contribute to the development of innovative materials with improved performance and functionality.
Used in Medicinal Chemistry Research:
2-(METHYLSULFONYL)-1-[3-(TRIFLUOROMETHYL)PHENYL]ETHANONE exhibits interesting pharmacological properties, making it a valuable target for medicinal chemistry research. Its study can lead to a better understanding of its potential therapeutic applications and the discovery of new drugs with novel mechanisms of action.

Check Digit Verification of cas no

The CAS Registry Mumber 128306-96-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,8,3,0 and 6 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 128306-96:
(8*1)+(7*2)+(6*8)+(5*3)+(4*0)+(3*6)+(2*9)+(1*6)=127
127 % 10 = 7
So 128306-96-7 is a valid CAS Registry Number.
InChI:InChI=1/C8H4BrF13/c9-2-1-3(6(14,15)16,7(17,18)19)4(10,11)5(12,13)8(20,21)22/h1-2H2

128306-96-7SDS

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-methylsulfonyl-1-[3-(trifluoromethyl)phenyl]ethanone

1.2 Other means of identification

Product number -
Other names -

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:128306-96-7 SDS

128306-96-7Downstream Products

128306-96-7Relevant academic research and scientific papers

SPIROUREA DERIVATIVES

-

Page/Page column 94, (2021/11/06)

The invention relates to compounds of Formula (I) wherein X1, X2, X3, Y, R1, R2A, R2B, R3, and R4 are as described in the description; to their preparation, to pharmaceutically acceptable salts thereof, to pharmaceutical compositions containing one or more compounds of Formula (I), and to the use of such compounds as medicaments, especially as Kv7 openers.

Iron(III)-catalyzed aerobic oxidation and cleavage/formation of a C-S bond

Shi, Xiaokang,Ren, Xiaoyu,Ren, Zhiyong,Li, Jian,Wang, Yuling,Yang, Sizhuo,Gu, Jixiang,Gao, Qiang,Huang, Guosheng

supporting information, p. 5083 - 5088 (2014/08/18)

A new iron(III)-catalyzed synthesis of β-oxo sulfones is described that employs vinylarenes and readily available dimethyl sulfoxide (DMSO) with hydrazine and oxygen as the oxidant. The reaction tolerates various functional group substituents on the vinylarene substrates to afford β-oxo sulfones in moderate to good yields. The cleavage and formation of the C-S bond are the key steps of this transformation.

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