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(E)-2-(3-(trifluoromethyl)styryl)quinoline is a complex organic compound characterized by a quinoline ring system, which is a tricyclic, polycyclic aromatic compound. The molecule features a styryl group, which is a vinylbenzene moiety, attached to the quinoline at the 2-position. The styryl group itself has a trifluoromethyl group (-CF3) at the 3-position, which introduces a significant electron-withdrawing and steric effect. (E)-2-(3-(trifluoromethyl)styryl)quinoline is of interest in various fields, including medicinal chemistry and materials science, due to its potential applications in the development of new drugs and advanced materials. The specific arrangement of atoms and the presence of the trifluoromethyl group can significantly influence the compound's chemical reactivity, physical properties, and potential biological activity.

450-70-4

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450-70-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 450-70-4 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,5 and 0 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 450-70:
(5*4)+(4*5)+(3*0)+(2*7)+(1*0)=54
54 % 10 = 4
So 450-70-4 is a valid CAS Registry Number.

450-70-4Downstream Products

450-70-4Relevant academic research and scientific papers

NaCl as Catalyst and Water as Solvent: Highly E-Selective Olefination of Methyl Substituted N-Heteroarenes with Benzyl Amines and Alcohols

Hazra, Susanta,Tiwari, Vikas,Verma, Ashutosh,Dolui, Pritam,Elias, Anil J.

, p. 5496 - 5501 (2020)

Oxidative coupling of benzylamines and alcohols with methyl substituted N-heteroarenes such as quinolines and quinoxalines has been achieved using chloride, a sea abundant anion as the catalyst for practical synthesis of a wide range of E-disubstituted olefins in aqueous medium. Detailed mechanistic studies and control experiments were carried out to deduce the reaction mechanism which indicated that in situ formed ClO2- is the active form of the catalyst. We have successfully carried out a 1 g scale reaction using this methodology, and five pharmaceutically relevant conjugated olefins were also synthesized by this method in moderate to good yields.

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