93049-43-5

Upstream product

• 106-48-9 4-chloro-phenol 
• 937-64-4 4-chlorophenyl chlorothionoformate 

Downstream Products

• 35082-55-4 6-(4-chloro-phenoxy)-2,2,2-tri-piperidin-1-yl-2H-2λ⁵-[1,3,4,5,2]thiatriazaphosphinine 
• 35045-32-0 6-(4-chloro-phenoxy)-hexa-N-ethyl-2λ⁵-[1,3,4,5,2]thiatriazaphosphinine-2,2,2-triamine 
• 1124-59-0 4-chlorophenyl cyanate 
• 35040-56-3 6-(4-chloro-phenoxy)-2,2,2-tri-morpholin-4-yl-2H-2λ⁵-[1,3,4,5,2]thiatriazaphosphinine 

Relevant academic research and scientific papers

Episulfidation of strained cycloalkenes in the thermolysis of 5-aryloxy-1,2,3,4-thiatriazoles

The thermolysis of 5-aryloxythiatriazoles 1 in the presence of norbornene (2a) and trans-cyclooctene (trans-2b) affords the corresponding thiiranes 3a and trans-3b in moderate yields. First-order kinetics are observed, suggesting that a sulfur intermediate, presumably dinitrogen sulfide, is generated in the fragmentation process of 1, which then serves as the active sulfur atom donor.