1297501-89-3

Upstream product

• 1297502-13-6 2,4,6-triethyl-1,3,5-tri{[(2-methoxycarbonylethyl)-sulfinyl]methyl}benzene 
• 220472-99-1 (2,4,6-triethylbenzene-1,3,5-triyl)trimethanethiol 
• 102-25-0 1,3,5-triethylbenzene 
• 181058-08-2 1,3,5-tris(bromomethyl)-2,4,6-triethylbenzene 

Downstream Products

• 1297501-95-1 2,4,6-triethyl-1,3,5-tri-{[(pyridine-2-yl)dithio]methyl}benzene 
• 1297501-96-2 2,4,6-triethyl-1,3,5-tri-{[(pyridine-4-yl)dithio]methyl}benzene 
• 1297502-12-5 1,3,5-tri({[(R)-2-tert-butoxycarbonylamino-2-methoxycarbonylethyl]dithio}methyl)-2,4,6-triethylbenzene 
• 1297501-91-7 1,3,5-tri-{[(4-aminopyrimidine-2-yl)dithio]methyl}-2,4,6-triethylbenzene 

Relevant academic research and scientific papers

From transient sulfenic acids to disulfide-functionalized tripodal structures

The condensation of transient polysulfenic acids with thiols, some of which containing privileged structures, has been applied to the synthesis of tripodal disulfides. The easy access to this new kind of conformationally constrained polyfunctionalized com