19495-07-9

Upstream product

• 75-15-0 carbon disulfide 
• 14212-38-5 bis(4-chlorophenyl)methanamine 
• 90-98-2 4,4'-Dichlorobenzophenone 
• 6306-46-3 1-[bromo(4-chlorophenyl)methyl]-4-chlorobenzene 
• 90-97-1 4,4'-dichlorobenzophenone 
• 3480-85-1 (4,4'-Dichlor-benzhydryl)-thiocyanat 

Downstream Products

• 144267-27-6 4,4-di-p-chlorophenylthiazolidine-2,5-dithione 
• 144267-32-3 1-hydroxy-4,4-di-p-chlorophenylimidazolidine-2,5-dithione 
• 144267-50-5 4,4-di-p-chlorophenyl-5-n-pentadecylthio-2,3-(4H)-dihydroimidazole-2-thione 
• 144267-37-8 4,4-di-p-chlorophenyl-1-palmitoyloxy-imidazolidine-2,5-dithione 
• 1370633-22-9 (S)-1-(di-p-chlorophenylmethyl)-3-(1-(diphenylphosphino)-3-phenylpropan-2-yl)thiourea 
• 110331-01-6 N-Cyclohexyl-N'-(4,4'-dichlor-benzhydryl)-thioharnstoff 
• 3480-85-1 (4,4'-Dichlor-benzhydryl)-thiocyanat 

Relevant academic research and scientific papers

The invention of radical reactions. Part XXVI. New thio- and seleno-hydroxamic acids; radical chemistry of their O-acyl derivatives

New thio- and seleno-hydroxamic acids have been synthesized from various 4,4-disubstituted thiazolidine 2,5-dithiones. Their corresponding O-acyl derivatives rearrange photochemically, with visible light, in an identical manner to the acyl derivatives of

Benzhydryl guanidines

Benzhydryl derivatives of guanidine (Formula I) having blood sugar lowering activity; pharmaceutical hypoglycemic compositions thereof and methods of administering same to hyperglycemic individuals.