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132719-10-9

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132719-10-9 Usage

Description

Ethanone, 1-(3,5-dimethylphenyl)-2,2,2-trifluoro(9CI) is a chemical compound with the molecular formula C11H11F3O. It is a derivative of acetophenone with the addition of a trifluoromethyl group. This colorless liquid with a strong odor is known for its flammability and volatility, requiring careful handling and adherence to safety protocols in laboratory or industrial settings.

Uses

Used in Organic Synthesis:
Ethanone, 1-(3,5-dimethylphenyl)-2,2,2-trifluoro(9CI) serves as a valuable reagent in organic synthesis, leveraging its unique properties to facilitate various chemical reactions and the formation of new compounds.
Used in Pharmaceutical Research:
In the pharmaceutical industry, this compound plays a crucial role in research and development. Its distinctive structure and properties make it a promising candidate for the creation of new drugs and medicinal agents, contributing to advancements in healthcare and treatment options.

Check Digit Verification of cas no

The CAS Registry Mumber 132719-10-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,2,7,1 and 9 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 132719-10:
(8*1)+(7*3)+(6*2)+(5*7)+(4*1)+(3*9)+(2*1)+(1*0)=109
109 % 10 = 9
So 132719-10-9 is a valid CAS Registry Number.
InChI:InChI=1/C10H9F3O/c1-6-3-7(2)5-8(4-6)9(14)10(11,12)13/h3-5H,1-2H3

132719-10-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(3,5-dimethylphenyl)-2,2,2-trifluoroethanone

1.2 Other means of identification

Product number -
Other names 3',5'-dimethyl-2,2,2-trifluoroacetophenone

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:132719-10-9 SDS

132719-10-9Downstream Products

132719-10-9Relevant articles and documents

Copper-Mediated Trifluoroacetylation of Arenediazonium Salts with Ethyl Trifluoropyruvate

Wu, Wei,Tian, Qinli,Chen, Taotao,Weng, Zhiqiang

supporting information, p. 16455 - 16458 (2016/11/11)

A copper-mediated trifluoroacetylation of various arenediazonium salts with ethyl trifluoropyruvate is reported. The reaction proceeded smoothly under mild conditions at room temperature giving trifluoromethyl aryl ketones in moderate to good yields. A variety of functional groups, including methoxy, hydroxy, ester, ketone, trifluoromethyl, and halide groups, were well tolerated. A possible reaction mechanism involving an aryl radical intermediate was proposed and supported by experimental evidence. This reaction provides a new route to trifluoromethyl aryl ketones, notable synthetic targets, from the corresponding anilines.

Photoaffinity labeling on magnetic microspheres (PALMm) methodology for topographic mapping: Preparation of PALMm reagents and demonstration of biochemical relevance

Halbfinger, Efrat,Gorochesky, Karine,Levesque, Sebastien A.,Beaudoin, Adrien R.,Sheihet, Larisa,Margel, Shlomo,Fischer, Bilha

, p. 2821 - 2832 (2007/10/03)

Photoaffinity labeling (PAL) is a technique widely used for identifying the binding-site within proteins. Although the classic method is both versatile and powerful, it suffers significant disadvantages, such as the need to radiolabel the PAL ligand, and the need to conduct highly complicated separations of both the labeled protein and the labeled peptides derived from it. Here, we propose a novel and universal methodology - Photo-Affinity Labeling on Magnetic microspheres (PALMm) designed to simplify and shorten the PAL protocol. In this context, we describe the preparation of PALMm reagents and the evaluation of their biochemical relevance regarding two ATP-binding enzymes: hexokinase and apyrase.

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