17583-16-3 Usage
Chemical structure
Thiazole derivative with a benzene ring and a methoxy group
The compound features a thiazole ring (a five-membered ring with one sulfur atom and one oxygen atom) fused to a benzene ring (a six-membered ring with alternating single and double bonds). A methoxy group (-OCH3) is attached to the phenyl moiety (a benzene ring with a hydrogen atom replaced by a side chain).
Biological properties
Potential pharmacological activities
2-(4-methoxyphenyl)-5,6-dihydrobenzo[d]thiazol-7(4H)-one has been studied for its potential biological properties, including anti-inflammatory and analgesic effects, which may contribute to the development of new drugs for various medical conditions.
Scientific research
Ongoing investigation of specific properties and potential uses
Researchers continue to study the compound to better understand its specific properties, potential applications, and possible uses in the development of new drugs for a range of medical conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 17583-16-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,5,8 and 3 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 17583-16:
(7*1)+(6*7)+(5*5)+(4*8)+(3*3)+(2*1)+(1*6)=123
123 % 10 = 3
So 17583-16-3 is a valid CAS Registry Number.
17583-16-3Relevant articles and documents
Versatile approaches to a library of building blocks based on 5-acylthiazole skeleton
Kulyk, Olesia G.,Biloborodov, Dmytro A.,Cherevatenko, Maksim A.,Shyriakin, Yevhen Y.,Lyapunov, Alexander Yu.,Mazepa, Alexander V.,Vashchenko, Valerii V.,Orlov, Valeriy D.,Kolosov, Maksim A.
, p. 3616 - 3628 (2020)
Thiazole derivatives represent an important class of azole heterocycles with a broad spectrum of biological activity and, therefore, the synthesis of these compounds is of remarkable concern. We present here practical and reliable protocol for synthesis of some 5-acylthiazoles and demonstrate their utility in the preparation of several new series of thiazole-containing building blocks through transformation of 5-acyl function. Specifically, thiazole-based alcohols, oximes, primary, and secondary amines were successively synthesized in good to excellent yields. The chemical structures of obtained compounds were confirmed by 1H and 13C NMR-spectroscopy, elemental analysis, and mass-spectrometry.
