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Carbetapentane

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Identification
Molecular formula
C17H24ClNO2
CAS number
104-31-4
IUPAC name
(1-ethyl-3-piperidyl)methyl N-(2-chloro-6-methyl-phenyl)carbamate
State
State

At room temperature, carbetapentane is a solid.

Melting point (Celsius)
108.00
Melting point (Kelvin)
381.15
Boiling point (Celsius)
365.50
Boiling point (Kelvin)
638.65
General information
Molecular weight
283.84g/mol
Molar mass
282.7900g/mol
Density
1.1500g/cm3
Appearence

Carbetapentane is typically found as a white to off-white crystalline powder.

Comment on solubility

Solubility of (1-ethyl-3-piperidyl)methyl N-(2-chloro-6-methyl-phenyl)carbamate

The solubility of (1-ethyl-3-piperidyl)methyl N-(2-chloro-6-methyl-phenyl)carbamate in different solvents can vary significantly based on its chemical structure. Here are some key points to consider:

  • Polarity: This compound, due to the presence of both polar (carbamate) and nonpolar (ethyl and phenyl groups) functional groups, exhibits a moderate level of polarity. Thus, it may be more soluble in polar organic solvents such as methanol, ethanol, or acetone compared to nonpolar solvents.
  • Temperature Dependence: Like many organic compounds, the solubility of this carbamate can be influenced by temperature, generally increasing at higher temperatures.
  • pH Sensitivity: The solubility behavior may also change with pH, particularly if the compound ionizes under different acid-base conditions, affecting its ability to dissolve.

It’s crucial to conduct solubility tests in various solvents to precisely determine the solubility profile of this compound for practical applications.

Interesting facts

Interesting Facts about (1-ethyl-3-piperidyl)methyl N-(2-chloro-6-methyl-phenyl)carbamate

(1-ethyl-3-piperidyl)methyl N-(2-chloro-6-methyl-phenyl)carbamate is a fascinating compound in the realm of organic chemistry, particularly within the field of pharmacology. This compound showcases the intricate union of aromatic and aliphatic structures, paving the way for several intriguing properties and applications.

Noteworthy Characteristics

  • Pharmaceutical Relevance: This compound exhibits potential as a pharmaceutical agent, particularly in the development of therapies for neurological disorders.
  • Mechanism of Action: Compounds similar to this one often function as enzyme inhibitors, suggesting possible roles in modulating neurotransmitter levels.
  • Structure-Activity Relationship: The unique combination of the piperidine ring and the carbamate functionality demonstrates how minor structural variations can lead to significant changes in biological activity.
  • Synthesis Challenges: The synthesis of such intricate molecules often requires advanced synthetic methodologies, showcasing the ingenuity of modern organic chemists.

As an illustration of how chemistry can intertwine with various disciplines, this compound could serve as a *case study* for students learning about:

  • Organic synthesis techniques
  • Medicinal chemistry
  • Drug design and development

In the words of renowned chemist, "The subtle nuances of organic compounds often hold the key to transformative discoveries." This is especially true for (1-ethyl-3-piperidyl)methyl N-(2-chloro-6-methyl-phenyl)carbamate, where understanding its structure can unlock new avenues in medicinal research.

Ultimately, the exploration of this compound exemplifies the ongoing journey within chemistry to discover and optimize new materials that can significantly impact health and well-being.

Synonyms
2-Chloro-6-methylcarbanilic acid (1-ethyl-3-piperidyl)methyl ester
20930-88-5
BRN 1488619
DTXSID60943222
CARBANILIC ACID, 2-CHLORO-6-METHYL-, (1-ETHYL-3-PIPERIDYL)METHYL ESTER
(1-Ethylpiperidin-3-yl)methyl hydrogen (2-chloro-6-methylphenyl)carbonimidate