68013-99-0

Upstream product

• 532-55-8 Benzoyl isothiocyanate 
• 34551-29-6 4-methyl-5-phenylimino-Δ²-1,2,3,4-thiatriazoline 
• 126806-25-5 5-methylimino-3-(p-nitrophenyl)imino-4-phenyl-1,2,4-thiadiazolidine 
• 13078-30-3 phenyl-[1,2,3,4]thiatriazol-5-yl-amine 
• 68013-96-7 3-Benzoylimino-5-methylimino-4-phenyl-1,2,4-dithiazolidine 
• 2131-61-5 p-nitrophenyl isothiocyanate 

Relevant academic research and scientific papers

Mechanism of the Cycloaddition-Elimination Reactions of 4-methyl-5-phenylimino-Δ3-1,2,3,-thiatriazoline with Alkyl and Aryl Isothiocyanates

The formation of thiadiazolidines 3a-c and dithiazolidines 4a-c and 5a-b from the title reactions has been studied in detail under a variety of conditions.On the basis of kinetic measurements, isomerizations studies and cross experiments a mechanism is pr

CYCLOADDITION-ELIMINATION REACTIONS OF 4-METHYL-5-PHENYLIMINO-Δ2-1,2,3,4-THIATRIAZOLINE WITH STRONG ELECTROPHILIC ISOTHIOCYANATES. MECHANISM OF THE ISOMERIZATION PROCESS

The 3,5-bis(substituted)imino-1,2,4-dithiazolidines (2), obtained from 4-alkyl-5-arylimino-1,2,3,4-thiatriazolines and isothiocyanates, rearrange to isomeric 3,5-bis(substituted)imino-1,2,4-dithiazolidines (3) by way of a cycloaddition-elimination reactio