943642-53-3

Upstream product

• 943642-52-2 2-amino-1,3,4-thiadiazino[6,5-b]-indole 
• 100-52-7 benzaldehyde 
• 91-56-5 indole-2,3-dione 
• 1165809-20-0 indole-2,3-dione 3-thiosemicarbazone 

Downstream Products

• 1266319-22-5 C₁₆H₁₀N₄S*C₄₂H₇₀O₃₅ 

Relevant academic research and scientific papers

A comparative study of inclusion complexes of orthosubstituted [arylidenamino]-1,3,4-thiadiazino[6,5b] indole derivatives

Some[Arylidenamino]-1,3,4-thiadiazino[6,5b] indoles have been synthesized starting from indole-2,3-dione, thiosemicarbazide and aromatic aldehydes with activating and deactivating groups. Inclusion complexes of these compounds have been prepared with β-cy

Thermodynamic and spectral studies of inclusion complexes of substituted indole derivatives with β-cyclodextrin

Indole and its analogous are very good pharmacophores for designing several chemotherapeutic reagents which exhibit wide spectrum of antimicrobial activities. The poor solubility of these compounds in polar medium is one of the limiting factors for better

Synthesis of some substituted azetidinonyl and thiazolidinonyl-1,3,4- thiadiazino[6,5-b]indoles as prospective antimicrobial agents

Several 2-[(3-chloro-2-substituted phenyl)-4-azetidinon-3-yl]-1,3,4- thiadiazino[6,5-b]indoles and 2-[(2-substituted phenyl)-4-thiazolidinon-3-yl]-1, 3,4-thiadiazino[6,5-b]indoles have been synthesized. The structures of the synthesized compounds are char