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2-Fluoro-N-[2-(trifluoromethyl)phenyl]benzamide, 97%, is a high-purity organic compound with the molecular formula C15H10F4NO. It is a derivative of benzamide, featuring a fluorine atom at the 2-position and a trifluoromethyl group attached to the 2-position of the phenyl ring. This chemical is known for its potential applications in the synthesis of pharmaceuticals and agrochemicals, particularly as an intermediate in the development of new compounds with specific biological activities. The 97% purity indicates that the product is of high quality, with minimal impurities, which is crucial for its use in sensitive chemical reactions and applications where purity is essential.

2053-94-3

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2053-94-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2053-94-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,0,5 and 3 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 2053-94:
(6*2)+(5*0)+(4*5)+(3*3)+(2*9)+(1*4)=63
63 % 10 = 3
So 2053-94-3 is a valid CAS Registry Number.

2053-94-3Downstream Products

2053-94-3Relevant academic research and scientific papers

Experimental and computational analysis of supramolecular motifs involving Csp2(aromatic)-F and CF3 groups in organic solids

Panini, Piyush,Gonnade, Rajesh G.,Chopra, Deepak

, p. 4981 - 5001 (2016/07/06)

A detailed experimental (SCXRD) and theoretical (PIXEL and QTAIM) investigation of the evolution of different supramolecular motifs formed via the presence of both C(sp2)/(sp3)-F groups in the crystal packing has been performed in a

A strategy of employing aminoheterocycles as amide mimics to identify novel, potent and bioavailable soluble epoxide hydrolase inhibitors

Shen, Hong C.,Ding, Fa-Xiang,Deng, Qiaolin,Xu, Suoyu,Tong, Xinchun,Zhang, Xiaoping,Chen, Yuli,Zhou, Gaochao,Pai, Lee-Yuh,Alonso-Galicia, Magdalena,Roy, Sophie,Zhang, Bei,Tata, James R.,Berger, Joel P.,Colletti, Steven L.

experimental part, p. 5716 - 5721 (2010/04/30)

Distinct from previously reported urea and amide inhibitors of soluble epoxide hydrolase (sEH), a novel class of inhibitors were rationally designed based on the X-ray structure of this enzyme and known amide inhibitors. The structure-activity relationshi

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