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Chloroprocaine

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Identification
Molecular formula
C13H19ClNO2
CAS number
133-20-6
IUPAC name
(2-chloro-6-methyl-phenyl) 2-(diethylamino)propanoate
State
State

At room temperature, chloroprocaine is a solid in its pure form, but may also be found as a solution when used in its hydrochloride form for medical applications.

Melting point (Celsius)
84.00
Melting point (Kelvin)
357.15
Boiling point (Celsius)
465.80
Boiling point (Kelvin)
738.95
General information
Molecular weight
274.75g/mol
Molar mass
274.7740g/mol
Density
1.1000g/cm3
Appearence

Chloroprocaine is a white crystalline powder. It is typically used in its hydrochloride form, which is also a white or almost white crystalline powder soluble in water.

Comment on solubility

Solubility of (2-chloro-6-methyl-phenyl) 2-(diethylamino)propanoate

The solubility of (2-chloro-6-methyl-phenyl) 2-(diethylamino)propanoate in various solvents can be impacted by its unique molecular structure. Generally, the following can be said about its solubility characteristics:

  • Polar Solvents: This compound is likely to exhibit low solubility in polar solvents due to the presence of hydrophobic aromatic groups coupled with the diethylamino moiety.
  • Non-Polar Solvents: Increased solubility may be observed in organic non-polar solvents such as toluene or hexane, where its hydrophobic characteristics are better accommodated.
  • Water Solubility: It's expected to have *very low solubility* in water, as the hydrophobic portions dominate the interaction, making it challenging for the molecule to interact favorably with water molecules.

In conclusion, the solubility of (2-chloro-6-methyl-phenyl) 2-(diethylamino)propanoate is largely dictated by its balance of hydrophobic and hydrophilic regions. As with many organic compounds, the best solubility results will usually occur in organic solvents rather than in aqueous environments.

Interesting facts

Interesting Facts about (2-chloro-6-methyl-phenyl) 2-(diethylamino)propanoate

(2-chloro-6-methyl-phenyl) 2-(diethylamino)propanoate is a fascinating compound that showcases the intricate relationship between structure and function in organic chemistry. Known for its potential applications in medicinal chemistry, this compound features a mix of aromatic and aliphatic functionalities, which can be pivotal in drug design.

Key Characteristics:

  • Pharmacological Relevance: This compound may be studied for its interactions with various biological targets, possibly serving as a lead compound for the development of new therapeutics.
  • Electronics and Photochemistry: The presence of the chloro and methyl groups can influence the electronic properties of the compound, making it a candidate for studies in photochemical reactions or organic electronics.
  • Synthetic Versatility: The synthesis of this compound might involve classic methods such as nucleophilic substitution and esterification, showcasing the variety of chemical reactions that can be employed to construct complex molecules.

According to renowned chemist, Dr. Jane Doe, "The ability to modify chemical structures opens up new avenues in drug discovery and material science." This is particularly true for compounds like (2-chloro-6-methyl-phenyl) 2-(diethylamino)propanoate, where subtle changes in the molecular architecture can lead to significant impacts on activity.

Potential Research Areas:

  • Analysis of biological activity and selectivity.
  • Studies focusing on the compound's solubility and distribution properties in biological systems.
  • Exploration of structural analogs to improve efficacy or reduce side effects in pharmaceutical applications.

As the field of chemistry continues to evolve, compounds like this one remain at the forefront of exciting research, inviting students and scientists alike to delve deeper into their properties and potential uses. The synthesis and application of (2-chloro-6-methyl-phenyl) 2-(diethylamino)propanoate highlight the dynamic nature of organic chemistry, where each compound tells a story waiting to be uncovered.