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(3-Amino-4-phenyl-6-p-tolyl-thieno[2,3-b]pyridin-2-yl)-(4-fluoro-phenyl)-methanone is a complex organic compound with a molecular formula of C25H18FN3OS. It features a thieno[2,3-b]pyridine core, which is fused with a pyridine ring, and is adorned with an amino group at the 3-position, a phenyl group at the 4-position, and a p-tolyl group (a tolyl group with a para-methyl substitution) at the 6-position. The compound also includes a 4-fluoro-phenyl group attached to a methanone (ketone) functionality. This chemical structure suggests potential applications in medicinal chemistry, possibly as a precursor to pharmaceuticals or as a compound with biological activity. The specific properties and uses of (3-Amino-4-phenyl-6-p-tolyl-thieno[2,3-b]pyridin-2-yl)-(4-fluoro-phenyl)-methanone would depend on its stability, solubility, and interaction with biological targets, which are not detailed in this summary.

94360-95-9

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94360-95-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 94360-95-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,4,3,6 and 0 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 94360-95:
(7*9)+(6*4)+(5*3)+(4*6)+(3*0)+(2*9)+(1*5)=149
149 % 10 = 9
So 94360-95-9 is a valid CAS Registry Number.

94360-95-9Downstream Products

94360-95-9Relevant academic research and scientific papers

CYCLIZATION OF NITRILES. IX. SYNTHESES BASED ON 2-ARYL-3-AROYL-1,1-DICYANOPROPANES

Shestopalov, A. M.,Promonenkov, V. K.,Sharanin, Yu. A.,Rodinovskaya, L. A.,Sharanin, S. Yu.

, p. 1382 - 1401 (2007/10/02)

2-Aryl-3-aroyl-1,1-dicyanopropanes and 2-aryl-3-aroyl-1-bromo-1,1-dicyanopropanes were synthesized from chalcones and malononitrile and were converted into 4,6-diaryl-2-bromo-3-cyanopyridines and 3-cyano-2(1H)-pyridinethiones.The 2-aryl-3-aroyl-1-bromo-1,1-dicyanopropanes proved convenient intermediates for the production of the corresponding cyclopropanes and other compounds.By their reaction with urea a new method was developed for the production of substituted 3-cyano-2(1H)-pyridinethiones.The 2-bromo-3-cyanopyridines contain a mobile bromine atom readily exchanged for the various nucleophilic residues of alcohols and amines and for iodide, and cyano and thiocyanato groups.The 3-cyano-2(1H)-pyridinethiones were used in the synthesis of 3-aminothienopyridines through the isolated 2-Z-methylthio-3-cyanopyridines.

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