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Chlorphenesin carbamate hydrochloride

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Identification
Molecular formula
C14H19Cl2N2O3
CAS number
37098-63-2
IUPAC name
2-piperidin-1-ium-1-ylethyl N-(4-chlorophenyl)carbamate;chloride
State
State

At room temperature, chlorphenesin carbamate hydrochloride is a solid. It is often stored in a dry environment to maintain its stability and prevent moisture absorption.

Melting point (Celsius)
174.00
Melting point (Kelvin)
447.15
Boiling point (Celsius)
397.00
Boiling point (Kelvin)
670.15
General information
Molecular weight
360.26g/mol
Molar mass
360.2550g/mol
Density
1.1400g/cm3
Appearence

Chlorphenesin carbamate hydrochloride typically appears as a white to off-white crystalline powder. It is known for its fine texture and is often found in a highly purified form.

Comment on solubility

Solubility of 2-piperidin-1-ium-1-ylethyl N-(4-chlorophenyl)carbamate; chloride

The solubility of 2-piperidin-1-ium-1-ylethyl N-(4-chlorophenyl)carbamate; chloride is a topic of interest due to its potential applications in various fields. This compound, characterized by both a piperidinium moiety and a carbamate function, presents a unique solubility profile that can impact its usability.

Factors Influencing Solubility

Several factors contribute to the solubility behavior of this compound:

  • Ionic Nature: The presence of the chloride ion enhances water solubility through ion-dipole interactions.
  • Molecular Structure: The hydrogen-bonding potential and the overall polarity of the compound play crucial roles in its dissolution in polar solvents.
  • Temperature: Like many compounds, increased temperature can facilitate solubility, enabling better interaction with solvent molecules.

General Solubility Insights

In a solvent like water, one might expect:

  • This compound to be fairly soluble due to the ability of the ionic component to interact favorably with solvent molecules.
  • However, the presence of bulky aromatic groups can hinder complete solubility, resulting in partial dissolution depending on concentration.

In conclusion, while it can be anticipated that 2-piperidin-1-ium-1-ylethyl N-(4-chlorophenyl)carbamate; chloride exhibits a reasonable degree of solubility in polar solvents, the intricate balance between its ionic and non-ionic characteristics leads to variable solubility outcomes. Understanding these subtleties is key for researchers and practitioners working with this compound.

Interesting facts

Interesting Facts About 2-Piperidin-1-ium-1-ylethyl N-(4-chlorophenyl)carbamate;chloride

This compound, often referred to in scientific literature, represents a fascinating intersection of organic chemistry and pharmacology. Here are some compelling insights:

  • Structure and Function: The presence of a piperidine ring alongside the carbamate structure suggests that this compound may have significant biological activity, potentially acting as a pharmacological agent in various therapeutic areas.
  • Chlorine's Role: The inclusion of a chlorine atom attached to the phenyl group hints at enhanced lipophilicity, which can influence the compound's interaction with biological systems, potentially improving its pharmacokinetic properties.
  • Research Potential: Compounds like this one are pivotal in drug design. Researchers may employ such structures to develop new pharmaceuticals or to understand the mechanisms of drug action.
  • Active Ingredients: The carbamate functional group is often found in insecticides and herbicides, highlighting the versatility of this compound in agricultural applications, aside from its medical potential.

As you delve deeper into the chemistry behind this compound, consider the following:

  1. How does the piperidine structure contribute to the stability of the compound?
  2. What are the possible synthetic routes for creating this compound in a laboratory setting?
  3. In which notable studies has this compound been featured, and what were the findings?

In conclusion, 2-piperidin-1-ium-1-ylethyl N-(4-chlorophenyl)carbamate;chloride is not just a simple chemical entity; it encapsulates a wealth of knowledge and potential, making it a significant subject for further research.

Synonyms
20229-03-2
p-Chlorocarbanilic acid 2-piperidinoethyl ester hydrochloride
K 496
CARBANILIC ACID, p-CHLORO-, 2-PIPERIDINOETHYL ESTER, HYDROCHLORIDE