66439-07-4

Upstream product

• 54012-74-7 10-(hydrazinoacetyl)-10H-phenothiazine 
• 100-52-7 benzaldehyde 

Downstream Products

• 129303-88-4 C₂₇H₁₉Cl₂N₅OS 
• 129320-57-6 C₂₈H₂₃N₅OS 
• 1218784-21-4 [2-phenyl-4-oxo-3-[{2-oxo-2-(phenothiazin-10-yl)ethyl}amino]-1,3-thiazolidin-5-yl]ethanoic acid 
• 129304-00-3 2-(phenothiazin-10-ylcarbonylmethyl)-2,5-diphenyl-2H-tetrazolium chloride 
• 129303-87-3 10-<α-(1,3-diphenylformazan-5-yl)acetyl>-10H-phenothiazine 
• 129303-95-3 10-<α-(3-chloro-2-oxo-4-phenyl-1-azetidinylamino)acetyl>-10H-phenothiazine 

Relevant academic research and scientific papers

Synthesis of phthalimido or succinimido-[2-aryl-4-oxo-3-[{2-oxo-2- (phcnothiazin-10-yl)ethyl}amino]-1,3-thiazolidin-5-yl]ethanoate and their antimicrobial activities

Keeping in view the pharmacological potential of thiazolidinones and phenothiazines, the title compounds containing these nuclei have been synthesized. Reaction of 10-(chloroacclyl)phcnolhiazinc 1 with hydrazine hydrate gives 10(hydrazinoacetyl)phenothiaz

Synthesis of 2′-aryl-3-N10-[(acetylamino)-1-3-thiazolidin- 4-ones] and 5′-arylidine-2-aryl-3-N10-[(acetylamino)-1,3- thiazolidin-4-ones] and their antimicrobial and diuretic activities

Thirty-nine new phenothiazino-4-oxo-thiazolidines and their 5-arylidines were synthesized and evaluated for their antimicrobial and diuretic activity. The structure of all the products was corroborated by IR, 1H NMR, mass spectra and elemental analysis. Some of the newly synthesized compounds show promising antimicrobial and diuretic activity.

Synthesis and antimicrobial activity of 4-oxothiazolidines, 4-oxoazetidines, malonanilic acid hydrazines and pyrazolin derivatives of phenothiazines

Several 10--10H-phenothiazines (IIIa-o), 1,3,7,9-tetrabromo-10--10H-phenothiazines (IVa-o), 1,3,7,9-tetrabromo-10-(N-arylmalonamic acid hydrazidoacetyl)-10H-ph