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(E)-2-(4-Chloro-phenyl)-3-thiophen-2-yl-acrylic acid is a complex organic compound characterized by its molecular formula C13H9ClOS. This conjugated molecule features a 4-chlorophenyl group attached to a 2-acrylic acid moiety, which is further connected to a thiophene ring. The "E" configuration indicates that the double bonds in the molecule are in the trans (E) geometric isomerism. (E)-2-(4-Chloro-phenyl)-3-thiophen-2-yl-acrylic acid is known for its potential applications in the synthesis of pharmaceuticals and other organic compounds due to its unique structure and reactivity. It is important to note that handling and disposal of such chemicals should be done with care, adhering to safety protocols, due to their potential reactivity and the presence of a chlorine atom, which can affect stability and toxicity.

50626-16-9

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50626-16-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 50626-16-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,0,6,2 and 6 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 50626-16:
(7*5)+(6*0)+(5*6)+(4*2)+(3*6)+(2*1)+(1*6)=99
99 % 10 = 9
So 50626-16-9 is a valid CAS Registry Number.

50626-16-9Downstream Products

50626-16-9Relevant academic research and scientific papers

THE MASS SPECTRA OF SOME (E)- AND (Z)-α-(PHENYL)-β-(2-THIENYL)ACRYLAMIDES

Amato, M. E.,Fisichella, S.,Occhipinti, S.,Scarlata, G.

, p. 35 - 40 (2007/10/02)

Mass spectra of some (E)- and (Z)-α-(4-X-phenyl)-β-(2-thienyl) acrylamides at 70 eV are reported.The stereoisomeric compounds do not show significant differences.The mass spectra show a four centre reaction scheme with NH2 migration to the β-carbon atom and subsequent fission of Cα-Cβ bond.

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