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(E)-1-phenyl-N-(2-(trifluoromethyl)phenyl)methanimine is an organic compound characterized by its unique molecular structure. It features a phenyl group attached to a methanimine moiety, which is a nitrogen-containing functional group. The methanimine nitrogen is bonded to a phenyl ring and a 2-(trifluoromethyl)phenyl group, the latter being a phenyl ring with a trifluoromethyl substituent at the 2-position. (E)-1-phenyl-N-(2-(trifluoromethyl)phenyl)methanimine is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals due to its reactivity and the presence of the electron-withdrawing trifluoromethyl group, which can influence the compound's electronic properties and reactivity. The (E)-configuration indicates the geometric isomerism around the double bond, which is an important aspect of its stereochemistry.

344-61-6

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344-61-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 344-61-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,4 and 4 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 344-61:
(5*3)+(4*4)+(3*4)+(2*6)+(1*1)=56
56 % 10 = 6
So 344-61-6 is a valid CAS Registry Number.

344-61-6Relevant academic research and scientific papers

Synthesis of 1,2-dihydropyridines using vinyloxiranes as masked dienolates in imino-aldol reactions

Brunner, Bernhard,Stogaitis, Nicole,Lautens, Mark

, p. 3473 - 3476 (2007/10/03)

The application of vinyloxiranes, substituted with an electron-withdrawing group, as masked dienolates in vinylogous imino-aldol reactions was achieved. Under the reaction conditions highly substituted 1,2-dihydropyridines were obtained in moderate to good yields. Mechanistic studies indicate that the reaction proceeds via the formation of an (E)-amino-α,β-unsaturated aldehyde, followed by isomerization to the (Z)-isomer, cyclization, and elimination of a water molecule, leading to the formation of the 1,2-dihydropyridine.

SYNTHESE VON FLUORIERTEN N-ARYLAMINO-ARYLMETHANPHOSPHONSAEUREDIALKYLESTERN

Gruss, Ulrike,Haegele, Gerhard

, p. 209 - 222 (2007/10/02)

Fluorinated α-C- and N-arylsubstituted aminomethanephosphonic acid diethylesters 5 are prepared in high yields by a "two-step" procedure: mixing equimolar amounts of fluorinated benzaldehydes 1 and anilines 2 to benzaldehyde-(N-aryl-)imines 3.Subsequently

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