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Methylphenidate

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Identification
Molecular formula
C14H19NO2
CAS number
1919-14-8
IUPAC name
1-(4-methoxyphenyl)-2-(1-piperidylimino)ethanone
State
State

At room temperature, methylphenidate is in a solid state, in the form of a crystalline powder. It is stable under normal conditions and should be stored away from strong oxidizing agents.

Melting point (Celsius)
92.50
Melting point (Kelvin)
365.65
Boiling point (Celsius)
338.80
Boiling point (Kelvin)
611.95
General information
Molecular weight
233.31g/mol
Molar mass
233.3060g/mol
Density
1.1960g/cm3
Appearence

Methylphenidate typically appears as a white to off-white, crystalline powder. It is visually characterized by its relatively fine grain size and uniform texture. It is not significantly hygroscopic.

Comment on solubility

Solubility of 1-(4-methoxyphenyl)-2-(1-piperidylimino)ethanone

The solubility of 1-(4-methoxyphenyl)-2-(1-piperidylimino)ethanone can be influenced by several factors, highlighting its behavior in different solvents:

  • Polarity: This compound contains both polar and nonpolar functional groups. Its methoxy group adds to its polar characteristics, which may enhance solubility in polar solvents like ethanol and water.
  • Hydrogen bonding: The ability of the molecule to engage in hydrogen bonding can increase its solubility in protic solvents. If the solvent can donate and accept hydrogen bonds effectively, solubility is likely to improve.
  • Hydrophobic interactions: The presence of the piperidine ring suggests that less polar, nonpolar solvents like chloroform or dichloromethane may also dissolve this compound effectively.
  • Temperature dependence: As with many chemical compounds, solubility can increase with temperature. Heating the solvent may be necessary to fully dissolve this compound when working with less favorable solvents.

In summary, the solubility of 1-(4-methoxyphenyl)-2-(1-piperidylimino)ethanone is determined by a complex interplay of its molecular structure and the nature of the solvent used. Understanding these solubility characteristics can aid in practical applications and experimental procedures.

Interesting facts

1-(4-Methoxyphenyl)-2-(1-piperidylimino)ethanone: Interesting Facts

This compound, 1-(4-methoxyphenyl)-2-(1-piperidylimino)ethanone, is quite fascinating due to its structural components and the functions they afford it. Here are some engaging insights:

  • Structural Diversity: The unique combination of a methoxyphenyl group and a piperidine ring contributes to notable chemical stability and reactivity patterns, situating this compound in a unique niche of organic chemistry.
  • Pharmacological Potential: Compounds with similar structural features often exhibit biological activity, leading to significant interest in their potential applications in pharmaceuticals, particularly as medicinal agents.
  • Mechanisms of Action: The imine structure within its framework can facilitate various reactions, possibly acting as a site for nucleophilic attack in biochemical processes—an attribute that makes 1-(4-methoxyphenyl)-2-(1-piperidylimino)ethanone a compelling candidate for further research.
  • Synthetic Utility: The relatively straightforward synthesis of compounds like this allows chemists to explore a variety of derivatives, making them excellent building blocks for larger, more complex molecules.

In the realm of organic synthesis, the versatility of 1-(4-methoxyphenyl)-2-(1-piperidylimino)ethanone exemplifies the intricate balance of structure and function in chemical compounds. As stated by many chemists, "The beauty of organic chemistry lies not only in its complexity but in the simplicity of its building blocks."

This compound showcases how a single chemical entity can pave the way for expansive research prospects in medicinal chemistry and beyond, highlighting the continuous journey of discovery in the field of chemistry.