916497-79-5

Upstream product

• 21095-40-9 4-(octyloxy)benzene-1-sulfonyl chloride 
• 102231-96-9 p-octyloxybenzenethiol 
• 4163-65-9 per-O-acetyl-α-D-mannopyranose 

Downstream Products

• 916497-93-3 Acetic acid (2R,4aR,6R,7S,8S,8aR)-8-benzyloxy-6-(4-octyloxy-phenylsulfanyl)-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-7-yl ester 
• 916497-84-2 (2R,4aR,6R,7S,8R,8aR)-8-Benzyloxy-6-(4-octyloxy-phenylsulfanyl)-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-7-ol 
• 916497-88-6 (3aS,4R,5aR,8R,9aR,9bS)-4-(4-Octyloxy-phenylsulfanyl)-2,8-diphenyl-hexahydro-[1,3]dioxolo[4',5':4,5]pyrano[3,2-d][1,3]dioxine 
• 916497-86-4 (2R,3S,4S,5S,6R)-2-Hydroxymethyl-6-(4-octyloxy-phenylsulfanyl)-tetrahydro-pyran-3,4,5-triol 

Relevant academic research and scientific papers

Odorless benzenethiols in synthesis of thioglycosides and its application for glycosylation reactions

p-Octyloxybenzenethiol (2) was synthesized as a new odorless benzenethiol. Moreover, preparation of thioglycosides using 2 and their application for glycosylation reactions were attempted. As a result, it was found that the thioglycosides were as excellen