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3-[5-(2-fluoro-phenyl)-thiophen-2-yl]-acrylic acid is a complex organic compound characterized by its unique molecular structure. It features a thiophene ring, which is a five-membered aromatic ring with one sulfur atom, and a phenyl ring, which is a six-membered aromatic ring. The thiophene ring is substituted at the 5-position with a 2-fluoro-phenyl group, and the phenyl ring has a fluorine atom at the 2-position. The acrylic acid moiety, which is a vinylogous carboxylic acid, is attached to the thiophene ring at the 3-position. 3-[5-(2-fluoro-phenyl)-thiophen-2-yl]-acrylic acid is of interest in the field of organic chemistry and may have potential applications in the development of pharmaceuticals or materials science due to its specific structural features.

949977-46-2

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949977-46-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 949977-46-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,4,9,9,7 and 7 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 949977-46:
(8*9)+(7*4)+(6*9)+(5*9)+(4*7)+(3*7)+(2*4)+(1*6)=262
262 % 10 = 2
So 949977-46-2 is a valid CAS Registry Number.

949977-46-2Relevant academic research and scientific papers

Heteroaryl-substituted carboxamides and use thereof for the stimulation of the expression of NO synthase

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Page/Page column 42, (2008/12/06)

The present invention relates to heteroaryl-substituted carboxamides of the formula I, in which Het, A, X, R1, R2 and R3 have the meanings indicated in the claims, which modulate the transcription of endothelial nitric oxi

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