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2-((4-Fluorophenyl)thiomethyl)benzoic acid is a chemical compound with the molecular formula C14H11FO2S. It is a derivative of benzoic acid, featuring a fluorophenylthiomethyl group attached to the 2-position of the benzene ring. 2-<(4-Fluorophenyl)thiomethyl>benzoic acid is characterized by the presence of a fluorine atom in the para position of the phenyl ring, which can influence its electronic properties and reactivity. The thiomethyl group (-CH2S-) provides a sulfur atom that can participate in various chemical reactions, such as oxidation or nucleophilic substitution. 2-<(4-Fluorophenyl)thiomethyl>benzoic acid may be used in the synthesis of pharmaceuticals, agrochemicals, or other organic compounds due to its unique structural features.

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Check Digit Verification of cas no

The CAS Registry Mumber 728-98-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,2 and 8 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 728-98:
(5*7)+(4*2)+(3*8)+(2*9)+(1*8)=93
93 % 10 = 3
So 728-98-3 is a valid CAS Registry Number.

728-98-3Relevant academic research and scientific papers

Pyridazone derivative and its uses

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Paragraph 0158; 0161, (2022/01/12)

The present invention belongs to the pharmaceutical field, specifically relates to a pyridazone derivative and its uses, compounds thereof and pharmaceutically acceptable salts, solvates including hydrates, polycrystallines, prodrugs, co-crystallines, tau

Synthesis and biological activity of 11-[4-(cinnamyl)-1-piperazinyl]-6,11-dihydrodibenz[b,e]oxepin derivatives, potential agents for the treatment of cerebrovascular disorders

Kurokawa,Sato,Masuda,Yoshida,Ochi,Zushi,Fujiwara,Naruto,Uno,Matsumoto

, p. 2564 - 2573 (2007/10/02)

A series of 11-[4-(cinnamyl)-1-piperazinyl]-6,11-dihydrodibenz[b,e]oxepins and related compounds were synthesized and evaluated for their protective activities against complete ischemia, normobaric hypoxia, lipidperoxidation and convulsion. Structure-activity relationship studies of this series led to the finding of (E)-1-(3-fluoro-6,11-dihydrodibenz[b,e]oxepin-11-yl)-4-(3-phenyl-2-prop enyl)piperazine dimaleate (50), AJ-3941 with the most appropriate property for combined pharmacological activities. Compound 50 also shows an inhibitory effect against cerebral edema as well when orally given to rats.

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