155791-18-7

Upstream product

• 102871-39-6 phenyl(thiophen-3-yl)methanol 
• 18162-48-6 tert-butyldimethylsilyl chloride 
• 498-62-4 3-thiophene carboxaldehyde 
• 959399-22-5 C₁₇H₂₄OSSi 

Downstream Products

• 155791-24-5 4-(1-hydroxy-1-phenylmethyl)-2-thiophenesulfonamide 
• 155791-21-2 4-<1-(tert-butyldimethylsiloxy)-1-phenylmethyl>-2-thiophenesulfonamide 

Relevant academic research and scientific papers

Solvent-controlled Csp2→O silyl migration: The "one-pot" synthesis of 2,3-disubsituted thiophenes

(Chemical Equation Presented) An effective "one-pot" synthesis of disubstituted thiophene derivatives employing 3-bromo-2-silyl thiophenes has been developed. A solvent-controlled [1,4] Csp2→O silyl migration was involved as the key step in thi

Synthesis and carbonic anhydrase inhibitory activity of 4-substituted 2- thiophenesulfonamides

A series of 4-substituted 2-thiophenesulfonamides was prepared from 3- thiophenecarboxaldehyde using metalation chemistry developed for 3- furaldehyde. Several of these compounds inhibit carbonic anhydrase II in vitro at concentrations of less than 10 nM.