63559-46-6

Upstream product

• 139265-27-3 (S)-2,3-Dihydro-benzofuran-2-carboxylic acid 4-nitro-phenyl ester 

Downstream Products

• 139265-27-3 (S)-2,3-Dihydro-benzofuran-2-carboxylic acid 4-nitro-phenyl ester 
• 847948-99-6 (S)-7-Amino-2,3-dihydro-benzofuran-2-carboxylic acid methyl ester 
• 66673-53-8 Biphenyl-4-carboxylic acid (3aR,4R,5R,6aS)-4-((E)-(R)-3-(S)-2,3-dihydro-benzofuran-2-yl-3-hydroxy-propenyl)-2-oxo-hexahydro-cyclopenta[b]furan-5-yl ester 
• 66673-52-7 Biphenyl-4-carboxylic acid (3aR,4R,5R,6aS)-4-((E)-(S)-3-(S)-2,3-dihydro-benzofuran-2-yl-3-hydroxy-propenyl)-2-oxo-hexahydro-cyclopenta[b]furan-5-yl ester 
• 66673-50-5 Biphenyl-4-carboxylic acid (3aR,4R,5R,6aS)-4-((E)-3-(S)-2,3-dihydro-benzofuran-2-yl-3-oxo-propenyl)-2-oxo-hexahydro-cyclopenta[b]furan-5-yl ester 

Relevant academic research and scientific papers

Comparison of deacylation rates of chymotryptic catalysis within an enantiomeric pair of p-nitrophenyl esters

p-Nitrophenyl esters carrying a chiral acyl group were synthesized. These compounds were shown to meet the requirements of chymotrypsin for both the specific binding and the acylation. Therefore, the behavior of p-nitrophenyl esters with chymotrypsin is c