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Chlorphenesin carbamate

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Identification
Molecular formula
C15H21ClN2O2
CAS number
886-74-8
IUPAC name
2-(1-piperidyl)ethyl N-(2-chloro-6-methyl-phenyl)carbamate
State
State

At room temperature, chlorphenesin carbamate is in a solid state. It is typically stable and does not readily degrade or change state under normal environmental conditions.

Melting point (Celsius)
135.00
Melting point (Kelvin)
408.15
Boiling point (Celsius)
455.20
Boiling point (Kelvin)
728.40
General information
Molecular weight
316.80g/mol
Molar mass
316.7960g/mol
Density
1.1680g/cm3
Appearence

Chlorphenesin carbamate typically appears as a white to off-white crystalline powder. Its fine crystalline form may exhibit a slight sheen under light. The appearance can also vary slightly depending on the form in which it is prepared or processed for specific applications.

Comment on solubility

Solubility of 2-(1-piperidyl)ethyl N-(2-chloro-6-methyl-phenyl)carbamate

The solubility of 2-(1-piperidyl)ethyl N-(2-chloro-6-methyl-phenyl)carbamate can be quite interesting due to the characteristics of its molecular structure. Understanding solubility is fundamental in various applications including pharmaceuticals and chemical processing. Here are some factors to consider:

  • Polarity: As a carbamate derivative, the compound exhibits polar characteristics due to the presence of the carbamate functional group. This can enhance its solubility in polar solvents.
  • Hydrogen Bonding: The ability to form hydrogen bonds can significantly affect solubility. The amine group in the piperidine ring may facilitate interactions with water molecules, aiding in solubility.
  • Structural Influences: Bulky substituents like the chloromethyl group may hinder complete solvation, potentially impacting solubility in certain solvents.

It is important to note that the solubility of this compound may be significantly different in varied solvents. For instance:

  1. Water: The solubility may be limited due to hydrophobic interactions from the phenyl group.
  2. Organic Solvents: The compound might be more soluble in non-polar or less polar organic solvents, aligning with the overall hydrophobic nature of part of its structure.

In conclusion, while specific quantitative data may be limited, the solubility characteristics of 2-(1-piperidyl)ethyl N-(2-chloro-6-methyl-phenyl)carbamate highlight the intricate balance of polarity, hydrogen bonding ability, and structural factors that together determine its behavior in various environments.

Interesting facts

Interesting Facts about 2-(1-piperidyl)ethyl N-(2-chloro-6-methyl-phenyl)carbamate

This compound falls under the category of carbamates, which are notable for their diverse applications in both pharmaceuticals and agriculture. The structure of this compound features a piperidine ring, which contributes to its biological activity and significant pharmacological properties.

Key Features:

  • Pharmacological Importance: Compounds similar to 2-(1-piperidyl)ethyl N-(2-chloro-6-methyl-phenyl)carbamate are often explored for their potential use as therapeutic agents, particularly in the field of neuroscience, due to their ability to modulate neurotransmitter activity.
  • Environmental Relevance: As a carbamate, it may play a role in studies regarding agricultural chemistry where carbamates are commonly employed as pesticides, showcasing their importance in food production and pest management.
  • Synthetic Routes: The synthesis of carbamates is a fascinating area of study, often involving reactions with isocyanates. This compound's synthesis may include steps that highlight the reactivity of amines and alcohols in organic chemistry.
  • Structure-Activity Relationship: Understanding the relationship between the chemical structure and its biological activity can pave the way for the development of new drugs, making compounds like this one integral to medicinal chemistry.

The compound's name reveals a complex molecular architecture that suggests potential for specific interactions with biological targets. As a chemistry student or researcher, one can appreciate not just its functional groups, but also the intricate balance of chemical properties that make this compound both useful and interesting.

In summary, the exploration of 2-(1-piperidyl)ethyl N-(2-chloro-6-methyl-phenyl)carbamate opens doors to understanding the intricate world of carbamate chemistry and its critical role in modern science and technology.