4-Chlorophenylphenylcarbamate

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Identification

Molecular formula
C20H28ClN2O2
IUPAC Name
(2-piperidin-1-ium-1-ylcyclohexyl) N-(o-tolyl)carbamate;chloride
Molecular Weight
361.89g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.1368g/cm3
Synonyms
o-Methylcarbanilic acid 2-piperidinocyclohexyl ester hydrochloride
Interesting facts

Interesting Facts about (2-Piperidin-1-ium-1-ylcyclohexyl) N-(o-tolyl)carbamate; Chloride

This fascinating compound belongs to the class of carbamates, which are widely known for their applications in various fields such as agriculture, pharmaceuticals, and industrial chemistry. Here are some noteworthy insights:

  • Versatile Applications: Carbamates are utilized in pesticide formulation, as they are effective against a broad range of pests. The unique structure of this compound enhances its efficacy.
  • Biological Relevance: Compounds related to piperidine often exhibit interesting biological properties. They can act as neurotransmitter inhibitors and have potential in medicinal chemistry for developing therapeutics.
  • Structure-Activity Relationship: The incorporation of the o-tolyl group can influence the pharmacological properties of the compound, making it a subject of interest for research in drug design.
  • Cationic Characteristics: The presence of the piperidin-1-ium group suggests that this compound may exhibit cationic characteristics, which can aid in its interaction with biological membranes.
  • Research Potential: Due to its unique structure, scientists are keen to explore its *potential in material science* and as a *building block for synthesizing more complex molecules*.

In conclusion, (2-piperidin-1-ium-1-ylcyclohexyl) N-(o-tolyl)carbamate; chloride is not just another chemical entity; it is a compound with *multifaceted applications* and a rich field for ongoing research. As chemists delve deeper into its properties and functions, it promises to expand our understanding of carbamate chemistry and its diverse implications.

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