1304076-70-7

Upstream product

• 4093-29-2 methyl 4-(acetylamino)-o-anisate 
• 55304-05-7 4-acetylamino-2-methoxy-benzoic acid 

Downstream Products

• 908085-10-9 C₁₉H₁₈ClN₃O₄S 
• 1304076-77-4 4-chlorobenzal-(4'-acetamido-2'-methoxybenzoyl)hydrazine 
• 1304076-86-5 C₁₉H₁₉N₃O₄S 
• 1304076-74-1 benzal-(4'-acetamido-2'-methoxybenzoyl)hydrazine 
• 1304076-80-9 4-hydroxybenzal-(4'-acetamido-2'-methoxybenzoyl)hydrazine 
• 1304076-88-7 C₁₉H₁₉N₃O₅S 
• 1304076-83-2 4-methoxy-benzal-(4'-acetamido-2'-methoxybenzoyl)hydrazine 
• 1304076-92-3 C₂₀H₂₁N₃O₅S 
• 1304076-79-6 2-hydroxybenzal-(4'-acetamido-2'-methoxybenzoyl)hydrazine 
• 1304076-87-6 C₁₉H₁₉N₃O₅S 
• 908089-55-4 4-hydroxy-3-methoxy-benzal-(4'-acetamido-2'-methoxybenzoyl)hydrazine 
• 908085-25-6 C₂₀H₂₁N₃O₆S 

Relevant academic research and scientific papers

GLUCOSE-SENSITIVE PEPTIDE HORMONES

The present invention relates to a conjugate of the formula P-L-I, wherein P is a peptide hormone effecting the metabolism of carbohydrates in vivo, L is a hydrolysable linker molecule consisting of Lp and Li, and I is a molecule cap

Syntheses of some thiazolidin-4-ones as potential antimicrobial agents

4-Acetamido-2-methoxybenzoyl hydrazine (1) on condensation with different aromatic aldehydes yielded the substituted benzal-(4'- acetamido-2'- methoxybenzoyl)hydrazines (2a-f) which on cyclization with thioglycolic acid in presence of anhydrous aluminium chloride as catalyst afforded 2-(substituted phenyl)-3-(4'-acetamido-2'-methoxy benzamido)-5-H-thiazolidin-4-ones (3a-f). The structures of the newly synthesized compounds have been established by analytical and spectral methods. These compounds have also been screened for their biological activity.