Chlorhexidine

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Identification

Molecular formula
C22H30Cl2N10
CAS Number
55-56-1
IUPAC Name
[N'-[N'-[(4-chlorophenyl)methyl]carbamimidoyl]carbamimidoyl]ammonium;chloride
Molecular Weight
505.45g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.1630g/cm3
Interesting facts

Interesting Facts About N'-[N'-[(4-chlorophenyl)methyl]carbamimidoyl]carbamimidoyl]ammonium Chloride

N'-[N'-[(4-chlorophenyl)methyl]carbamimidoyl]carbamimidoyl]ammonium chloride is an intriguing compound that has caught the attention of chemists and researchers alike. Here are some fascinating insights about this compound:

  • Versatile Applications: This compound is known for its potential applications in medicinal chemistry, particularly in the synthesis of new drug candidates. Its unique structure might contribute to biological activity, making it a subject of interest in pharmacological studies.
  • Synthetic Pathways: The synthesis of this compound involves advanced organic chemistry techniques. Scientists utilize methods such as amide coupling and functional group transformations to create its complex structure.
  • Chlorine Atom Influence: The presence of the 4-chlorophenyl group in the molecule may enhance its biological activity. Chlorine substituents often play a critical role in modifying the properties of organic compounds, influencing their metabolism and activity within biological systems.
  • Stability Considerations: As with many ammonium salts, the stability of this compound can be attributed to ionic interactions. The ammonium cation interacts favorably with the chloride anion, contributing to its solid-state characteristics.

In summary, N'-[N'-[(4-chlorophenyl)methyl]carbamimidoyl]carbamimidoyl]ammonium chloride is more than just a chemical formula; it represents a rich landscape for scientific exploration. Researchers continue to investigate its properties and potential applications, highlighting the ongoing evolution of synthetic chemistry.

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