Skip to main content

4-Chlorophenylphenylcarbamate

ADVERTISEMENT
Identification
Molecular formula
C20H28ClN2O2
IUPAC name
(2-piperidin-1-ium-1-ylcyclohexyl) N-(o-tolyl)carbamate;chloride
State
State

At room temperature, this compound is typically solid due to its high melting point. It retains a stable form under normal conditions, displaying the robustness characteristic of crystalline solids.

Melting point (Celsius)
158.50
Melting point (Kelvin)
431.70
Boiling point (Celsius)
270.00
Boiling point (Kelvin)
543.00
General information
Molecular weight
361.89g/mol
Molar mass
361.8920g/mol
Density
1.1368g/cm3
Appearence

The compound typically presents as a crystalline solid and can vary from off-white to white in color. It is often seen in powdered or crystalline form, and like many crystalline substances, it possesses a reflective sheen.

Comment on solubility

Solubility Characteristics of (2-piperidin-1-ium-1-ylcyclohexyl) N-(o-tolyl)carbamate; chloride

The solubility of this compound, known as (2-piperidin-1-ium-1-ylcyclohexyl) N-(o-tolyl)carbamate; chloride, is influenced by several key factors:

  • Polarity: The presence of both an ionic component (the chloride ion) and a polar functional group can significantly enhance solubility in polar solvents such as water.
  • Hydrogen Bonding: The potential for hydrogen bonding with water molecules can further facilitate solvation, making the compound more soluble in aqueous solutions.
  • Temperature Dependence: Like many ionic compounds, solubility may increase with temperature, thus it’s essential to consider thermal effects when measuring solubility.
  • pH Influence: The pH of the solution can also play a crucial role; variations in acidity can lead to changes in the ionization of the compound, thus affecting its solubility.

Overall, the solubility of (2-piperidin-1-ium-1-ylcyclohexyl) N-(o-tolyl)carbamate; chloride is likely to be moderate to high in polar solvents due to the combination of ionic and polar characteristics. As the saying goes, "like dissolves like," illustrating that polar solvents typically dissolve ionic and polar solutes effectively.


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.

Synonyms
o-Methylcarbanilic acid 2-piperidinocyclohexyl ester hydrochloride
20186-58-7
K 1403
CARBANILIC ACID, o-METHYL-, 2-PIPERIDINOCYCLOHEXYL ESTER, HYDROCHLORIDE