New research progress on 125464-42-8 in 2021. In classical electrochemical theory, both the electron transfer rate and the adsorption of reactants at the electrode control the electrochemical reaction. 125464-42-8, Name is 3-Amino-2-(4-chlorophenyl)propane-1-sulfonic acid, molecular formurla is C9H12ClNO3S. In a document, author is Demirci, Serpil, introducing its new discovery. COA of Formula: https://www.ambeed.com/products/125464-42-8.html.
Thiomorpholine was converted to the corresponding 1,3,4-oxadiazole (4), arylidenehydrazide (5a-e), and 1,2,4-triazole (7a and, 7b) derivatives via the formation of hydrazide (3). Compounds 4 and 7 were next converted to the corresponding Mannich bases containing piperidin, beta-lactam, fluoroquinolone, piperazine, or morpholine core. Conventional and microwave-assisted methods were used for all syntheses. The effect of acid catalyst on Mannich reactions was also investigated. All the newly synthesized compounds were screened for their antimicrobial, antiglucosidase, antilipase, anti-urease, and antioxidant activities. Most exhibited good-moderate antibacterial and/or antifungal activity. Docking of some of the synthesized compounds into the active sites of lipase, alpha-glucosidase, and urease was carried out in order to predict the binding affinities and noncovalent interactions stabilizing the enzyme-ligand complexes. Docking results complemented well the experimental results on inhibitory effects of compounds. Higher binding affinities were observed for active compounds in contrary to inactive ones.
The result showed that such a combination of chemo- and biocatalysis improved the catalytic yield more than two times compared with that of sole metal catalysis.you can check my other blog about 125464-42-8, you can contact me at any time and look forward to more communication. COA of Formula: https://www.ambeed.com/products/125464-42-8.html.
Reference:
Thiomorpholine – Wikipedia,
,Thiomorpholine | C4H9NS – PubChem