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3-[5-(4-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 4-fluoro-phenyl group, and the phenyl ring carries a fluorine atom at the 4-position. The acrylic acid moiety, which is a vinylogous carboxylic acid, is attached to the 3-position of the thiophene ring. 3-[5-(4-fluoro-phenyl)-thiophen-2-yl]-acrylic acid is known for its potential applications in the pharmaceutical industry, particularly as a building block for the synthesis of various drugs and medicinal compounds. Its specific properties, such as its reactivity and potential biological activity, make it a subject of interest for researchers in the field of organic chemistry and drug development.

929975-30-4

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929975-30-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 929975-30-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,2,9,9,7 and 5 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 929975-30:
(8*9)+(7*2)+(6*9)+(5*9)+(4*7)+(3*5)+(2*3)+(1*0)=234
234 % 10 = 4
So 929975-30-4 is a valid CAS Registry Number.

929975-30-4Relevant 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 41, (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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