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2-(2,4-dimethoxy-phenyl)-3c-(3,4-dimethoxy-phenyl)-acrylic acid is a complex organic compound characterized by its unique molecular structure. It features a central acrylic acid backbone, with two phenyl rings attached at the 2nd and 3rd carbon positions. These phenyl rings are substituted with methoxy groups at the 2,4-positions on the first ring and the 3,4-positions on the second ring. This chemical is known for its potential applications in various fields, such as pharmaceuticals and materials science, due to its specific electronic and steric properties. The compound's structure endows it with unique chemical reactivity and physical characteristics, making it a subject of interest for researchers in organic chemistry and related disciplines.

6586-21-6

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6586-21-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6586-21-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,5,8 and 6 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 6586-21:
(6*6)+(5*5)+(4*8)+(3*6)+(2*2)+(1*1)=116
116 % 10 = 6
So 6586-21-6 is a valid CAS Registry Number.

6586-21-6Relevant academic research and scientific papers

ACID CATALYZED ISOMERIZATION OF Z-α-PHENYLCINNAMIC ACIDS AND THEIR CONVERSION TO ISOMERIC ISOAURONES

Gadre, S. Y.,Marathe, K. G.

, p. 1015 - 1028 (2007/10/02)

E(4') and Z(4)-α-phenylcinnamic acids were synthesized.These were been converted into isoaurones.The stereochemistry of these were determined by 1H NMR and Lanthanide induced shift (LIS) studies.

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