13202-32-9

Upstream product

• 16914-21-9 3-benzyl-2-benzylsulfanyl-4-methyl-thiazolium; bromide 
• 1950-26-1 benzylammonium N-benzyldithiocarbamate 
• 78-95-5 chloroacetone 
• 4209-18-1 3-(1-phenylmethyl)-4-methylthiazol-3-ium chloride 
• 75-15-0 carbon disulfide 
• 100-46-9 benzylamine 

Downstream Products

• 55379-26-5 benzyl-(3-benzyl-4-methyl-3H-thiazol-2-ylidene)-amine 
• 77008-06-1 C₁₁H₁₀⁽²⁾HNS₂ 
• 55019-82-4 3-benzyl-4-methyl-2-methylsulfanyl-thiazolium; iodide 
• 55379-19-6 3-benzyl-4-methyl-2-(4-nitro-benzylsulfanyl)-thiazolium; bromide 
• 16914-21-9 3-benzyl-2-benzylsulfanyl-4-methyl-thiazolium; bromide 

Relevant academic research and scientific papers

Electrogenerated base promoted synthesis of N-substituted-4-hydroxy-4- methylthiazolidine-2-thione derivatives

Electrochemically-generated basic species from the reduction of acetonitrile assisted the condensation of carbon disulfide, primary arylmethylamines and chloroacetone to yield the corresponding N-substituted-4-hydroxy-4-methylthiazolidine-2-thione derivat

REACTION OF N-ALKYLTHIAZOLIUM HALIDES, INCLUDING THIAMINE, WITH SUPEROXIDE ION. CHEMISTRY AND BIOLOGICAL IMPLICATIONS.

N-alkylthiazolium halides are transformed by KO2 into the corresponding thiazolin-2-ones and thiazolin-2-thiones; the same reactions occur with thiamine, whose thiazolin-2-one pyrophosphate has been reported to be a strong inhibitor of pyruvic dehydrogenase.