116759-10-5 Usage
Description
4-(4-fluorophenyl)-2-[(E)-2-(4-methoxyphenyl)ethenyl]-1,3-thiazol-5-ylacetic acid is a complex organic compound characterized by a thiazole core structure with an acetic acid functional group. It features a fluoro-phenyl group and a methoxy-phenyl group, along with a double bond in the side chain, which contributes to its unique structural arrangement. Thiazole compounds, in general, are recognized for their wide range of biological activities, such as antimicrobial, antifungal, and anti-inflammatory properties. The specific structure of this compound hints at potential therapeutic uses, although further research is necessary to confirm its precise biological effects and applications.
Uses
Used in Pharmaceutical Industry:
4-(4-fluorophenyl)-2-[(E)-2-(4-methoxyphenyl)ethenyl]-1,3-thiazol-5-ylacetic acid is used as a potential therapeutic agent for various medical conditions due to its thiazole core structure and diverse functional groups. 4-(4-fluorophenyl)-2-[(E)-2-(4-methoxyphenyl)ethenyl]-1,3-thiazol-5-ylacetic acid's unique arrangement may offer novel interactions with biological targets, potentially leading to the development of new drugs with improved efficacy and selectivity.
Used in Chemical Research:
In the field of chemical research, 4-(4-fluorophenyl)-2-[(E)-2-(4-methoxyphenyl)ethenyl]-1,3-thiazol-5-ylacetic acid serves as a valuable compound for studying the structure-activity relationships of thiazole-based molecules. Its synthesis and modification can provide insights into the design of new molecules with enhanced biological activities and selectivity for specific targets.
Used in Material Science:
4-(4-fluorophenyl)-2-[(E)-2-(4-methoxyphenyl)ethenyl]-1,3-thiazol-5-ylacetic acid's structural features, including the thiazole ring and the presence of electron-withdrawing and electron-donating groups, may endow it with unique electronic and optical properties. As such, 4-(4-fluorophenyl)-2-[(E)-2-(4-methoxyphenyl)ethenyl]-1,3-thiazol-5-ylacetic acid could be explored for applications in material science, potentially serving as a component in the development of novel materials with specific properties for various applications, such as sensors or optoelectronic devices.
Check Digit Verification of cas no
The CAS Registry Mumber 116759-10-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,6,7,5 and 9 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 116759-10:
(8*1)+(7*1)+(6*6)+(5*7)+(4*5)+(3*9)+(2*1)+(1*0)=135
135 % 10 = 5
So 116759-10-5 is a valid CAS Registry Number.
