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Chlorphenesin Carbamate Hydrochloride

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Identification
Molecular formula
C14H19ClN2O2
CAS number
12901-61-4
IUPAC name
2-piperidin-1-ium-1-ylethyl N-(2-chloro-6-methyl-phenyl)carbamate;chloride
State
State

At room temperature, chlorphenesin carbamate hydrochloride is generally in a solid state. It is available as a crystalline powder and remains stable when stored in a cool, dry place.

Melting point (Celsius)
82.00
Melting point (Kelvin)
355.15
Boiling point (Celsius)
310.00
Boiling point (Kelvin)
583.15
General information
Molecular weight
288.77g/mol
Molar mass
288.2000g/mol
Density
1.1680g/cm3
Appearence

Chlorphenesin carbamate hydrochloride typically appears as a white crystalline powder. It has a characteristic odor and is hygroscopic in nature.

Comment on solubility

Solubility of 2-piperidin-1-ium-1-ylethyl N-(2-chloro-6-methyl-phenyl)carbamate; chloride

The solubility of 2-piperidin-1-ium-1-ylethyl N-(2-chloro-6-methyl-phenyl)carbamate; chloride presents an intriguing aspect that is heavily influenced by its molecular structure and the presence of charged functional groups. Understanding its solubility can be essential for applications in pharmaceuticals and chemical research.

Key Factors Influencing Solubility:

  • Ionic Nature: Being a quaternary ammonium compound, the positive charge significantly enhances solubility in polar solvents like water.
  • Hydrophobic Interactions: The presence of the aromatic ring from the chloro-substituted phenyl group may contribute to decreased solubility in non-polar solvents.
  • Temperature Dependency: As with many compounds, increased temperature generally increases solubility, especially for ionic compounds.

In summary, this compound likely exhibits:

  • High solubility in water due to its ionic characteristics.
  • Limited solubility in organic solvents, attributed to its hydrophobic regions.

As quoted in solubility studies, "The balance between hydrophilicity and hydrophobicity determines the solubility profile of a compound." Thus, exploring this equilibrium can shed light on the practical formulations involving 2-piperidin-1-ium-1-ylethyl N-(2-chloro-6-methyl-phenyl)carbamate; chloride.

Interesting facts

Interesting Facts about 2-Piperidin-1-ium-1-ylethyl N-(2-chloro-6-methyl-phenyl)carbamate; chloride

This compound is a fascinating example of a quaternary ammonium salt, which belongs to a broader class of chemical compounds known for their diverse applications in fields like pharmacology and agriculture. As a scientist, it’s exciting to delve deeper into its structure and potential uses.

Key Characteristics:

  • Functionality: This compound features a piperidine ring, which is significant because piperidine and its derivatives are often utilized in drug design due to their ability to interact well with biological targets.
  • Biological Activity: Compounds like this are studied for their potential pesticide properties, making them relevant in agricultural chemistry.
  • Chlorine Substituent: The presence of a chloro group on the aromatic ring increases aromatic reactivity and may contribute to enhanced biological activity or potency.

Quote from a study: “The incorporation of electron-withdrawing groups can significantly alter the pharmacokinetic properties of compounds, thus making them candidates of interest in medicinal chemistry.”

Potential Applications:

  • Medications: This compound could inspire new formulations in the search for effective pharmaceuticals.
  • Agricultural Chemicals: With its potential as an insecticide or herbicide, studying its action mechanisms could lead to greener alternatives in pest management.
  • Chemical Research: Researchers might explore its synthetic pathways and reactions with other compounds to develop new materials or catalysts.

Overall, the study of 2-piperidin-1-ium-1-ylethyl N-(2-chloro-6-methyl-phenyl)carbamate; chloride provides invaluable insights into the interactions between molecular structure and function, driving innovation in both medicinal and environmental chemistry.

Synonyms
2-Chloro-6-methylcarbanilic acid 2-piperidinoethyl ester hydrochloride
20228-98-2
K 488
CARBANILIC ACID, 2-CHLORO-6-METHYL-, 2-PIPERIDINOETHYL ESTER, HYDROCHLORIDE