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Carisoprodol

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Identification
Molecular formula
C15H22N2O4
CAS number
78-44-4
IUPAC name
2-(dimethylamino)ethyl N-(3-methoxyphenyl)-N-phenyl-carbamate
State
State

At room temperature, Carisoprodol is a solid in crystalline form.

Melting point (Celsius)
94.00
Melting point (Kelvin)
367.15
Boiling point (Celsius)
371.60
Boiling point (Kelvin)
644.80
General information
Molecular weight
260.33g/mol
Molar mass
260.3340g/mol
Density
1.0860g/cm3
Appearence

Carisoprodol is a white to off-white, crystalline powder. It is odorless and has a bitter taste.

Comment on solubility

Solubility of 2-(dimethylamino)ethyl N-(3-methoxyphenyl)-N-phenyl-carbamate

The solubility of 2-(dimethylamino)ethyl N-(3-methoxyphenyl)-N-phenyl-carbamate can be influenced by various factors, including its molecular structure and the presence of functional groups. Here are some insights into its solubility characteristics:

  • Polarity: This compound features an amine and carbamate group, which can contribute to its overall polarity, potentially enhancing solubility in polar solvents such as water.
  • Aromatic rings: The presence of the methoxy and phenyl groups may affect solubility by enhancing hydrophobic interactions, leading to lower solubility in polar solvents.
  • Solvent compatibility: It is likely soluble in organic solvents such as ethanol or acetone, which can dissolve both hydrophilic and hydrophobic components efficiently.

Generally, the solubility of complex organic compounds like this one must be empirically determined because theoretical predictions can be challenging. As a tip: assess solubility in a range of solvents to gain a comprehensive understanding of the compound’s behavior in various environments.

In summary, while the solubility profile of this carbamate derivative is expected to be moderate in polar solvents and stronger in non-polar ones, experimental determination is key to confirming these hypotheses.

Interesting facts

Interesting Facts about 2-(Dimethylamino)ethyl N-(3-Methoxyphenyl)-N-phenyl-Carbamate

This compound is a fascinating example of a synthetic organic molecule with potential applications in the field of medicinal chemistry. It belongs to the class of carbamates, which are known for their diverse biological activities. Here are some intriguing facts about this compound:

  • Biological Activity: Carbamates, including this compound, can exhibit a range of pharmacological effects. Some have been studied for their potential as antidepressants and for their roles in modulating neurotransmitter systems.
  • Structural Complexity: The presence of both dimethylamino and methoxyphenyl groups contributes to the compound's structural diversity, which can influence its interaction with biological targets and enhance its therapeutic potential.
  • Synthesis Challenges: The synthesis of such compounds often involves intricate multi-step processes, showcasing the skill required in organic synthesis. Chemists may use various methods, including protective group strategies, to construct the desired molecular architecture.
  • Potential Research Applications: Researchers may explore this compound as a lead structure for developing new drugs. Its unique functional groups may provide insights into creating more effective therapeutic agents.
  • Environmental Impact: As with many organic compounds, understanding its degradation and ecological footprint is crucial, especially if it finds therapeutic use or enters the environment through various pathways.

Overall, 2-(dimethylamino)ethyl N-(3-methoxyphenyl)-N-phenyl-carbamate showcases the beauty and complexity of organic chemistry, as well as the potential it holds for future drug discovery and development.

Synonyms
(m-Methoxyphenyl)phenylcarbamic acid 2-(dimethylamino)ethyl ester
23379-71-7
CARBANILIC ACID, m-METHOXY-N-PHENYL-, 2-(DIMETHYLAMINO)ETHYL ESTER
BRN 3414017
K 79
2-(Dimethylamino)ethyl m-methoxy-N-phenylcarbanilate
DTXSID60177929