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Tolperisone

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Identification
Molecular formula
C16H21NO2
CAS number
728-88-1
IUPAC name
(1-methylpyrrolidin-3-yl) N,N-diphenylcarbamate
State
State

At room temperature, Tolperisone is in a solid state.

Melting point (Celsius)
174.00
Melting point (Kelvin)
447.15
Boiling point (Celsius)
253.00
Boiling point (Kelvin)
526.15
General information
Molecular weight
245.32g/mol
Molar mass
245.3160g/mol
Density
1.2000g/cm3
Appearence

Tolperisone is typically obtained as a white or almost white crystalline powder. It is practically odorless and has a slightly bitter taste.

Comment on solubility

Solubility of (1-methylpyrrolidin-3-yl) N,N-diphenylcarbamate

The solubility of (1-methylpyrrolidin-3-yl) N,N-diphenylcarbamate can be quite intriguing, as it showcases various factors that influence its behavior in different solvents. While the specific solubility characteristics can vary, several general observations can be made:

  • Polarity: The presence of both pyrrolidine and diphenyl groups affects the overall polarity of the compound, suggesting that it may be more soluble in non-polar to moderately polar solvents.
  • Temperature Dependence: As with many organic compounds, the solubility could increase with temperature, making it important to consider how this compound would behave under varying thermal conditions.
  • Potential Solvents: Solvents such as ethyl acetate or dichloromethane may be more effective for dissolving this compound due to their similar polarities, while water solubility may be limited.
  • Impact of pH: The ionization of the compound could be influenced by the pH of the solution, potentially enhancing its solubility in acidic or basic environments.

Understanding the solubility of (1-methylpyrrolidin-3-yl) N,N-diphenylcarbamate is essential for its application in various chemical processes. As one study stated, "The solubility behavior often dictates the usability of a compound in synthetic chemistry and pharmaceuticals." Hence, an in-depth investigation into the solubility characteristics is crucial for effective utilization.

Interesting facts

Interesting Facts About (1-methylpyrrolidin-3-yl) N,N-diphenylcarbamate

(1-methylpyrrolidin-3-yl) N,N-diphenylcarbamate is a fascinating compound that has captured the interest of researchers in various fields. Here are some compelling points to consider:

  • Pharmacological Potential: This compound exhibits interesting pharmacological properties that may contribute to developments in medicine, particularly in the realm of neuropharmacology.
  • Structure-Activity Relationship: The unique pyrrolidine ring structure allows for extensive study of its effect on biological systems, making it a significant subject of inquiry in medicinal chemistry.
  • Versatile Applications: Research on similar carbamate derivatives suggests potential applications in agriculture for pest control and in pharmaceuticals for treating neurological disorders.
  • Heterocyclic Chemistry: As a member of the heterocyclic compounds, it plays a pivotal role in understanding the interactions of nitrogen-containing compounds in organic synthesis.
  • Synthetic Pathways: The synthesis of this compound provides an excellent case study for students learning about organic reactions and the importance of carbamate functional groups in drug design.

The exploration of (1-methylpyrrolidin-3-yl) N,N-diphenylcarbamate not only enhances our understanding of chemical properties but also opens doors for innovative applications. As stated in research studies, "The importance of carbamates in therapeutic and agricultural chemistry cannot be overstated." Therefore, this compound represents an exciting area of study for chemists and pharmacologists alike.

Synonyms
1-Methyl-3-pyrrolidyl N,N-diphenylcarbamate
UNII-8FQK50LYCX
8FQK50LYCX
AHR 0800
AHR-0800
1-Methyl-3-pyrrolidyl N,N-diphenylcarbamate, (+/-)-
Carbamic acid, diphenyl-, 1-methyl-3-pyrrolidinyl ester
739-62-8
Carbamic acid, N,N-diphenyl-, 1-methyl-3-pyrrolidinyl ester
Q27270342