84968-87-6

Upstream product

• 99-92-3 p-aminobenzophenone 
• 42288-24-4 4-Carboxymethylamino-acetophenon 
• 84968-84-3 N-nitroso-N-(4-acetylphenyl)glycine 

Downstream Products

• 84969-03-9 3-<4-<3-(4-methylphenyl)-1-oxo-2-propenyl>phenyl>sydnone 
• 84968-93-4 3-<4-<3-(4-chlorophenyl)-1-oxo-2-propenyl>phenyl>sydnone 
• 84968-94-5 3-<4-<3-(4-nitrophenyl)-1-oxo-2-propenyl>phenyl>sydnone 
• 84968-91-2 3-<4-<1-oxo-3-phenyl-2-propenyl>phenyl>sydnone 
• 84968-96-7 C₁₇H₁₂N₂O₄ 
• 62646-10-0 4-acetylphenylhydrazine 

Relevant academic research and scientific papers

Synthesis and antimicrobial activity of 3-(substituted-phenyl)-sydnones

3-(3 or 4-Acetylphenyl)-sydnones 7, 8 have been synthesized by formation of the glycines 3, 4, followed by nitrosation to 5, 6 and cyclization with acetic anhydride to sydnones. Sydnone derivatives carrying chalcone moieties 15, 16 were prepared by format

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