Downstream Synthetic Route Of 843666-40-0

Note that a catalyst decreases the activation energy for both the forward and the reverse reactions and hence accelerates both the forward and the reverse reactions. you can also check out more blogs about 843666-40-0. Quality Control of 18-(tert-Butoxy)-18-oxooctadecanoic acid.

Chemical engineers ensure the efficiency and safety of chemical processes, adapt the chemical make-up of products to meet environmental or economic needs, and apply new technologies to improve existing processes. 843666-40-0, Name is 18-(tert-Butoxy)-18-oxooctadecanoic acid, molecular formula is C22H42O4, Quality Control of 18-(tert-Butoxy)-18-oxooctadecanoic acid, belongs to benzisoxazole compound, is a common compound. In a patnet, author is Belavagi, Ningaraddi S., once mentioned the new application about 843666-40-0.

Novel classes of 3-(6-Aryl-5-phenylsulfanylimidazo[2,1-b][1,3,4]thiadiazol-2-yl-methyl)-benzo[d]isoxazoles (2a-f) and 3-(5-Benzenesulfonyl-6-arylimidazo[2,1-b][1,3,4] thiadiazol-2-yl-methyl)-benzo[d]isoxazoles (3a-f) have been synthesized. The sulfide derivatives (2a-f) were obtained by the nucleophilic substitution of bromo derivatives (1a-f) with thiophenols, and sulfone derivatives (3a-f) were obtained by the oxidation of 2a-f. All the newly synthesized compounds were characterized by elemental analysis, infrared, nuclear magnetic resonance, and mass spectroscopic data. Furthermore, these novel sulfide and sulfone derivatives were screened for their antibacterial and antifungal activities against various microorganisms.

Note that a catalyst decreases the activation energy for both the forward and the reverse reactions and hence accelerates both the forward and the reverse reactions. you can also check out more blogs about 843666-40-0. Quality Control of 18-(tert-Butoxy)-18-oxooctadecanoic acid.

Reference:
Benzisoxazole – Wikipedia,
,Benzisoxazole – an overview | ScienceDirect Topics