84968-90-1

Upstream product

• 99-92-3 p-aminobenzophenone 
• 84968-84-3 N-nitroso-N-(4-acetylphenyl)glycine 
• 42288-24-4 4-Carboxymethylamino-acetophenon 
• 84968-87-6 3-[3-acetyl]phenyl sydnone 

Downstream Products

• 886220-20-8 C₁₇H₁₀BrClN₂O₃ 
• 886220-17-3 4-bromo-3-[4-(3-phenylacryloyl)phenyl]sydnone 
• 886220-19-5 C₁₈H₁₃BrN₂O₄ 
• 886220-26-4 3-{4-[3-(4-bromo-phenyl)-acryloyl]-phenyl}-5-methyl-3H-[1,3,4]oxadiazol-2-one 
• 886220-25-3 3-{4-[3-(4-chloro-phenyl)-acryloyl]-phenyl}-5-methyl-3H-[1,3,4]oxadiazol-2-one 
• 886220-23-1 5-methyl-3-[4-(3-p-tolyl-acryloyl)-phenyl]-3H-[1,3,4]oxadiazol-2-one 
• 886220-21-9 C₁₇H₁₀Br₂N₂O₃ 
• 886220-18-4 C₁₈H₁₃BrN₂O₃ 

Relevant academic research and scientific papers

Synthesis and pharmacological evaluation of 1,5-benzothiazepine derivatives

A simple method for the synthesis of 1,5-benzothiazepines integrated with 5-methyl-2-oxo-3-phenyl-Δ4-1,3,4-oxadiazoles in 75-95% yield is devised. A comparison of microwave-accelerated reaction with conventional heating is also illustrated. Structures of

Transformation of the sydnone ring into oxadiazolinones. A convenient one-pot synthesis of 3-aryl-5-methyl-1,3,4-oxadiazolin-2-ones from 3- arylsydnones and their antimicrobial activity

3-Arylsydnones (Ia-u) have been converted into the corresponding 3-aryl- 5-methyl-1,3,4-oxadiazolin-2-ones (IIIa-u) by a single-step reaction with bromine in acetic anhydride. In the preliminary screening of all these compounds, the halogen-substituted de

Reactions of 3-(p-Acetylphenyl)sydnones: Part 1-Synthesis and Biological Evaluation of 3-(p-Acetylphenl)sydnone and Its Derivatives

3-(p-Acetylphenyl)sydnone (7) undergoes condensation with aryl aldehydes to give the corresponding cinnamoyl derivatives (11-25).The reaction of sydnones (7-9) with hydroxylamine, phenylhydrazine, dimethyl acetylene-dicarboxylate and bromine gives the ket