5685-15-4 Usage
Uses
Used in Pharmaceutical Industry:
(4,5-Dihydro-thiazol-2-ylsulfanyl)-acetic acid is used as a key intermediate for the development of new drugs and bioactive molecules due to its unique thiazole ring structure. This application is driven by the compound's potential pharmacological properties, which include anti-inflammatory and anti-bacterial activities.
Used in Agrochemical Industry:
In the agrochemical industry, (4,5-Dihydro-thiazol-2-ylsulfanyl)-acetic acid is used as a building block in the synthesis of various compounds with potential applications in pest control and crop protection. Its incorporation into these compounds leverages its pharmacological properties to enhance their effectiveness against harmful organisms.
Used in Chemical Research:
(4,5-Dihydro-thiazol-2-ylsulfanyl)-acetic acid serves as an important research tool in the field of organic chemistry, particularly in the study of thiazole derivatives and their potential applications. Its unique structure allows scientists to explore new synthetic pathways and develop novel compounds with a wide range of properties and applications.
Check Digit Verification of cas no
The CAS Registry Mumber 5685-15-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,6,8 and 5 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 5685-15:
(6*5)+(5*6)+(4*8)+(3*5)+(2*1)+(1*5)=114
114 % 10 = 4
So 5685-15-4 is a valid CAS Registry Number.
5685-15-4Relevant academic research and scientific papers
de la Concepción, Juan García,ávalos, Martín,Babiano, Reyes,Cintas, Pedro,Jiménez, José L.,Light, Mark E.,Palacios, Juan C.
, p. 1551 - 1560 (2017)
We report a combined experimental and computational study on the cycloadditions of bicyclic 1,3-thiazolium-4-olates, derived from thiazolidin-2-thiones, with asymmetrically-substituted acetylenes. These results provide further mechanistic insights into the above dipolar cycloadditions and enable an unequivocal characterization by NMR spectroscopy of regiochemical patterns as previous derivatives had substituents at both C-2 (in the dipole) and C-6 (in products). Accordingly, new dihydrothiazolopyrid-2-ones have been obtained from a thioisomünchnone lacking substitution at C-2. With the aim of assessing the steric hindrance as well as the facial stereoselection induced by a bulky group on the Si face (relative to C-7a) of the mesoionic heterocycle, a chiral thioisomünchnone has also been obtained along with the resulting optically active thiazolopyridones. A computational study of these particular cycloadditions, largely based on an NBO analysis, allowed us to evaluate the influence of substituents on intermolecular steric repulsions, charge transfers, as well as solvent effects.
