One of the major reasons for studying chemical kinetics is to use measurements of the macroscopic properties of a system, Safety of (S)-3-(4-(5-Bromo-2-chlorobenzyl)phenoxy)tetrahydrofuran, such as the rate of change in the concentration of reactants or products with time.In a article, mentioned the application of 915095-89-5, Name is (S)-3-(4-(5-Bromo-2-chlorobenzyl)phenoxy)tetrahydrofuran, molecular formula is C17H16BrClO2
An efficient production synthesis of the SGLT-2 inhibitor Empagliflozin (5) from acid 1 is described. The key tactical stage involves I/Mg exchange of aryl iodide 2 followed by addition to glucono lactone 3 in THF. Subsequent in situ treatment of the resulting lactol with HCl in MeOH produces beta-anomeric methyl glycopyranoside 4 which is, without isolation, directly reduced with Et3SiH mediated by AlCl3 as a Lewis acid in CH 2Cl2/MeCN to afford 5 in 50% overall yield. The process was implemented for production on a metric ton scale for commercial launch.
One of the oldest and most widely used commercial enzyme inhibitors is aspirin, Safety of (S)-3-(4-(5-Bromo-2-chlorobenzyl)phenoxy)tetrahydrofuran, which selectively inhibits one of the enzymes involved in the synthesis of molecules that trigger inflammation. you can also check out more blogs about 915095-89-5
Reference:
Tetrahydrofuran – Wikipedia,
Tetrahydrofuran | (CH2)3CH2O – PubChem