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Tolterodine

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Identification
Molecular formula
C22H31NO2
CAS number
124937-52-6
IUPAC name
(1-methylpyrrolidin-3-yl)methyl N-(o-tolyl)carbamate
State
State
Tolterodine is typically a solid at room temperature.
Melting point (Celsius)
108.00
Melting point (Kelvin)
381.15
Boiling point (Celsius)
368.70
Boiling point (Kelvin)
641.85
General information
Molecular weight
325.44g/mol
Molar mass
325.4380g/mol
Density
1.1400g/cm3
Appearence
Tolterodine appears as a white to off-white crystalline solid.
Comment on solubility

Solubility of (1-methylpyrrolidin-3-yl)methyl N-(o-tolyl)carbamate

The solubility of the compound (1-methylpyrrolidin-3-yl)methyl N-(o-tolyl)carbamate can be influenced by various factors, including its molecular structure and the presence of functional groups. Understanding its solubility behavior is essential for its applications in pharmaceuticals and other fields.

Key Factors Influencing Solubility:

  • Polarity: The structure of this compound contains polar functional groups, which may contribute to its solubility in polar solvents such as water and alcohols.
  • Hydrophobic Regions: The presence of the o-tolyl group introduces a hydrophobic segment that could hinder solubility in aqueous environments.
  • pH Sensitivity: The solubility may also vary with the pH of the solution due to potential ionization of the carbamate group.

General observations suggest that:

  • The compound is likely to exhibit better solubility in organic solvents compared to water.
  • Its solubility can be enhanced by the use of co-solvents or by manipulating the pH of the solution.

In summary, although (1-methylpyrrolidin-3-yl)methyl N-(o-tolyl)carbamate may have complex solubility characteristics due to its structural components, understanding these aspects allows for effective utilization in various chemical applications.

Interesting facts

Interesting Facts about (1-methylpyrrolidin-3-yl)methyl N-(o-tolyl)carbamate

(1-methylpyrrolidin-3-yl)methyl N-(o-tolyl)carbamate is a fascinating compound found in various branches of chemistry, particularly in medicinal chemistry and agrochemistry. Here are some noteworthy aspects of this intriguing molecule:

  • Structure and Function: This compound comprises a pyrrolidine ring, which is known for its role in enhancing biological activity. Its unique structure allows for interesting interactions with biological targets, making it a subject of study in drug design.
  • Potential Applications: Compounds similar to this one are often investigated for their potential use in pharmaceuticals. Their ability to act as inhibitors or modulators for certain enzymes makes them valuable in treating various diseases.
  • Carbamate Nature: The presence of the carbamate functional group (–OC(=O)–NH–) is significant due to its reactivity in organic synthesis and its role in improving medicinal properties. Carbamates can enhance drug stability and bioavailability.
  • Research Interest: Scientists are continually exploring variations of this compound to identify new derivatives with improved efficacy or reduced toxicity. Such research may lead to developments in both human medicine and agricultural applications.
  • Multifunctionality: The compound’s design allows it to be optimized for various activities, including neuroprotective properties or insecticidal effects, showcasing its versatility across different sectors.

As with many chemical compounds, understanding (1-methylpyrrolidin-3-yl)methyl N-(o-tolyl)carbamate requires a balance of synthetic knowledge and biological insights. This compound exemplifies the intricate dance between structure and function that is central to the world of chemistry.

Synonyms
o-Methylcarbanilic acid (1-methyl-3-pyrrolidinyl)methyl ester
20930-79-4
BRN 1470055
DTXSID70943213
CARBANILIC ACID, o-METHYL-, (1-METHYL-3-PYRROLIDINYL)METHYL ESTER
(1-Methylpyrrolidin-3-yl)methyl hydrogen (2-methylphenyl)carbonimidate