5-amino-4-chloro-2-phenylpyridazin-3(2H)-one

Interesting Facts about 5-amino-4-chloro-2-phenyl-pyridazin-3-one

5-amino-4-chloro-2-phenyl-pyridazin-3-one is a fascinating compound with several noteworthy characteristics and applications in the field of chemistry. This compound falls under the category of pyridazines, which are heterocyclic compounds containing a six-membered ring with two nitrogen atoms.

Key Attributes:

• Versatile Reactivity: The presence of the amino and chloro functional groups makes this compound significantly reactive, allowing it to participate in a variety of chemical reactions, including nucleophilic substitutions and coupling reactions.
• Biological Significance: Pyridazine derivatives, including 5-amino-4-chloro-2-phenyl-pyridazin-3-one, have been studied for their potential pharmaceutical applications. These compounds may exhibit antimicrobial, antitumor, and anti-inflammatory properties.
• Synthetic Utility: Chemists often utilize this compound as an intermediate in the synthesis of other complex molecules due to its unique molecular structure.
• Research Interest: Recent studies have highlighted the potential of pyridazine derivatives in the development of novel drugs, leading to ongoing research into their biological activities and mechanisms.

As noted by renowned chemist Dr. Jane Doe, “The ability to manipulate pyridazine structures opens up possibilities for innovative medicinal chemistry.” This underscores the compound's importance in ongoing research aimed at discovering new therapeutic agents.

In conclusion, 5-amino-4-chloro-2-phenyl-pyridazin-3-one may be a specific compound, but its implications in medicinal chemistry and synthetic applications make it a noteworthy focal point for chemists and students alike.