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Meclofenoxate

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Identification
Molecular formula
C9H11ClN2O
CAS number
51-68-3
IUPAC name
2-(3-amino-5-chloro-phenyl)-N-methyl-acetamide
State
State

At room temperature, Meclofenoxate is generally a solid. It requires suitable storage conditions to maintain this state and ensure its proper handling.

Melting point (Celsius)
122.00
Melting point (Kelvin)
395.15
Boiling point (Celsius)
375.00
Boiling point (Kelvin)
648.15
General information
Molecular weight
213.68g/mol
Molar mass
213.6770g/mol
Density
1.3795g/cm3
Appearence

This compound is typically found as a crystalline solid. Its appearance may vary from white to slightly off-white depending on purity and crystal size. It is important to handle this compound under appropriate conditions to maintain its integrity.

Comment on solubility

Solubility of 2-(3-amino-5-chloro-phenyl)-N-methyl-acetamide

2-(3-amino-5-chloro-phenyl)-N-methyl-acetamide is an intriguing compound with specific solubility characteristics worth exploring. When considering its solubility, several factors come into play:

  • Polar Nature: The presence of an amino group and a carbonyl group in its structure suggests that this compound is likely polar. Polar compounds typically have greater solubility in polar solvents such as water.
  • Hydrogen Bonding: The capability of forming hydrogen bonds, given the amine and carbonyl functional groups, enhances its interactions with solvents, potentially increasing its solubility.
  • Solvent Specificity: In addition to water, 2-(3-amino-5-chloro-phenyl)-N-methyl-acetamide may also exhibit solubility in organic solvents like methanol or ethanol, though the extent may vary.
  • Structural Considerations: The bulky aromatic ring may hinder solubility in certain non-polar solvents, thereby making it less soluble in such environments.

Overall, while 2-(3-amino-5-chloro-phenyl)-N-methyl-acetamide is expected to be soluble in polar solvents, the exact solubility can differ based on temperature and solvent conditions. Practical experiments are essential to accurately determine its solubility profile in various environments.

Interesting facts

Interesting Facts About 2-(3-amino-5-chloro-phenyl)-N-methyl-acetamide

2-(3-amino-5-chloro-phenyl)-N-methyl-acetamide, often known for its diverse applications in the realm of pharmaceuticals, is a fascinating compound. Here are some noteworthy insights:

  • Pharmacological Significance: This compound belongs to a class of molecules that exhibit potential pharmacological activities, making it a key interest in drug design and discovery.
  • Structure-Activity Relationship: The presence of both the amino and chloro groups on the phenyl ring plays a pivotal role in influencing the biological activity of the compound. Modifications to these substituents can lead to various activity profiles.
  • Research Context: Researchers are continuously studying this compound to uncover its mechanisms of action and explore its efficacy against specific disease targets, particularly within the fields of oncology and infectious diseases.
  • Biomedical Application: Compounds like 2-(3-amino-5-chloro-phenyl)-N-methyl-acetamide are often evaluated for their ability to inhibit certain enzymes or receptors, which is crucial in the treatment of various conditions.

Furthermore, it is essential to remember the importance of safety and regulatory compliance when working with chemical compounds in laboratory settings. As noted by experts, "Safety first is the motto of any successful chemist." This highlights the need for rigorous adherence to protocols when handling such compounds.

In conclusion, 2-(3-amino-5-chloro-phenyl)-N-methyl-acetamide represents just one example of how modifications in chemical structure can lead to profound implications in both research and application within the scientific community.