4-Chlorobenzohydrazide

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Identification

Molecular formula
C7H7ClN2O
CAS Number
7392-44-3
IUPAC Name
4-chlorobenzohydrazide
Molecular Weight
170.60g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.3900g/cm3
Synonyms
4-Chlorobenzohydrazide
Interesting facts

Interesting Facts about 4-Chlorobenzohydrazide

4-Chlorobenzohydrazide, a compound notable for its various applications, showcases a compelling blend of chemistry and functionality. Here are some intriguing aspects of this compound:

  • Versatile Applications: 4-Chlorobenzohydrazide is widely recognized for its role in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. Its structure allows for easy modification, making it a valuable intermediate for various chemical reactions.
  • Biological Activity: Research has suggested that 4-Chlorobenzohydrazide exhibits potential biological properties, including *antimicrobial* and *antioxidant* activities. These properties have sparked interest in the pharmaceutical field for developing new therapeutic agents.
  • Reactivity: The hydrazide functional group in 4-Chlorobenzohydrazide undergoes several types of reactions, such as hydrazone formation and acylation. These reactions expand its utility in synthetic organic chemistry, particularly in the construction of more complex molecules.
  • Environmental Significance: The compound's derivatives are often explored for their potential as biodegradable agents. As environmental concerns grow, compounds like 4-Chlorobenzohydrazide may lead the way in developing greener chemical processes.
  • Research Interest: Continuous studies are being conducted to explore the full scope of its reactivity and potential applications. The compound serves as a key player in the study of heterocyclic chemistry and materials science.

In summary, 4-Chlorobenzohydrazide is not just a compound of interest for its chemical properties but also serves as a stepping stone in advancing research in multiple fields. Its versatile applications and potential for innovative uses exemplify the dynamic nature of chemical studies.

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