Chlorphenamine

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Identification

Molecular formula
C16H19ClN2
CAS Number
113-92-8
IUPAC Name
N-[(4-chlorophenyl)-phenyl-methyl]-N',N'-diethyl-ethane-1,2-diamine
Molecular Weight
274.79g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.0815g/cm3
Synonyms
BRN 2867152
Interesting facts

Interesting Facts about N-[(4-chlorophenyl)-phenyl-methyl]-N',N'-diethyl-ethane-1,2-diamine

N-[(4-chlorophenyl)-phenyl-methyl]-N',N'-diethyl-ethane-1,2-diamine, often abbreviated for convenience, belongs to a category of compounds known for their versatile applications in various fields. Here are some captivating insights about this compound:

  • Biological Activity: This compound is of particular interest in medicinal chemistry due to its potential biological properties. It has been studied for its effects in antitumor and antimicrobial activity, making it a candidate for further research in pharmaceutical applications.
  • Chemical Structure: The structure includes a chlorophenyl group, which is significant because halogenated compounds often exhibit increased reactivity and enhanced biological activity. The presence of the ethyl diethylamine groups also allows for a variety of modifications that can alter its pharmacological properties.
  • Synthetic Pathways: The synthesis of this compound typically involves multiple stages, utilizing reactions such as amine alkylation and Schotten-Baumann reactions. Understanding these pathways is crucial for scientists aiming to optimize yield and purity in laboratory settings.
  • Research Applications: This compound serves as a valuable reference in the study of organic synthesis and medicinal chemistry, enhancing our understanding of how structural features influence biological effectiveness.

In summary, the compound N-[(4-chlorophenyl)-phenyl-methyl]-N',N'-diethyl-ethane-1,2-diamine stands at the intersection of chemistry and biology, making it a fascinating subject of study that showcases the intricate relationship between molecular structure and biological activity.

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