66085-20-9

Upstream product

• 19078-72-9 bromo(phenyl)acetyl chloride 
• 149-30-4 2-Mercaptobenzothiazole 
• 149-30-4 2-thioxo-3H-1,3-benzothiazole 
• 82323-46-4 phenylglyoxylic acid chloride p-toluenesulfonylhydrazone 
• 4870-65-9 2-bromophenylacetic acid 

Downstream Products

• 66085-27-6 2-ethyl-4-phenyl-(3ac,11bc)-3a,11b-dihydro-4H-4r,11ac-episulfano-benzo[4,5]thiazolo[3,2-a]pyrrolo[3,4-c]pyridine-1,3,5-trione 
• 66085-30-1 1-oxo-2-phenyl-1,2,3,4-tetrahydro-2r,4ac-episulfano-benzo[4,5]thiazolo[3,2-a]pyridine-3c,4t-dicarbonitrile 
• 120-78-5 di(benzothiazol-2-yl)disulfide 
• 78751-22-1 1-Benzolsulfonyl-6,7-dimethyl-3-phenyl-1,2-dihydrochinoxalin-2-on 
• 78751-23-2 6,7-Dimethyl-3-phenyl-1,2-dihydro-chinoxalin-2-on 
• 66085-25-4 2-phenyl-3,4-bis-trifluoromethyl-benzo[4,5]thiazolo[3,2-a]pyridin-1-one 
• 66085-23-2 Dimethyl 1-Oxo-2-phenylbenzothiazolo<3,2-a>pyridine-3,4-dicarboxylate 
• 66085-26-5 2,4-diphenyl-(3ac,11bc)-3a,11b-dihydro-4H-4r,11ac-episulfano-benzo[4,5]thiazolo[3,2-a]pyrrolo[3,4-c]pyridine-1,3,5-trione 

Relevant academic research and scientific papers

Antitrichomonal Activity of Mesoionic Thiazolopyridines

Screening of mesoionic compounds as potential electron acceptors by analogy with metronidazole led to the finding of in vitro antitrichomonal activity for anhydro-2-phenyl-3-hydroxythiazolopyridinium hydroxide (1).In a series of analogues, potent i

Carbenoid Intermediates in the Synthesis of Mesoionic Anhydro-4-hydroxythiazolium Hydroxides

α-(Tosylhydrazono)phenylacetyl chloride and N-monosubstituted thioamides in dry, non-protic solvents and in the presence of Et3N give representatives of the title mesoionic ring system in good to excellent yields; carbene or carbenoid type intermediates a