1379507-93-3

Upstream product

• 105-09-9 1,4-bis(mercaptomethyl)benzene 
• 1379507-96-6 1,4-di-{[(2-methoxycarbonylethyl)thio]methyl}benzene 

Downstream Products

• 1379507-88-6 1,4-di-{[(β-D-glucopyranosyl)dithio]methyl}benzene 
• 1379507-90-0 1,4-di-{[(β-D-galactopyranosyl)dithio]methyl}benzene 
• 1379507-87-5 1,4-di-{[(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)dithio]methyl}benzene 
• 1586047-32-6 1-{[(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)dithio]methyl}-4-{[(2-methoxycarbonylethyl)sulfinyl]methyl}benzene 

Relevant academic research and scientific papers

Pyrimidine-derived disulfides as potential antimicrobial agents: Synthesis and evaluation in vitro

Antibiotic resistance is a worldwide problem. The synthesis and evaluation of new antimicrobial compounds, without cytotoxicity against human cells, are highly desired. In this paper, the preparation of a class of pyrimidine-derived disulfides is describe

Synthesis and biological evaluation of a new class of glycoconjugated disulfides that exhibit potential anticancer properties

A synthetic strategy, based on the in situ generation of sulfenic acids and their thermolysis in the presence of thiols, was developed for obtaining a collection of polyvalent disulfides in which a benzene scaffold accommodates two or three flexible arms