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Fluorolintane

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Identification
Molecular formula
C17H20FNO2
CAS number
1539263-91-1
IUPAC name
1-(4-fluorophenyl)-2-(morpholinomethyl)hex-5-yn-1-one
State
State
Fluorolintane is a solid at room temperature, characterized by its crystalline appearance and white color.
Melting point (Celsius)
70.00
Melting point (Kelvin)
343.15
Boiling point (Celsius)
270.00
Boiling point (Kelvin)
543.15
General information
Molecular weight
273.33g/mol
Molar mass
273.3300g/mol
Density
1.1690g/cm3
Appearence

Fluorolintane typically appears as a white crystalline powder. The compound is solid at room temperature and is often observed in the form of fine particles or crystalline structures.

Comment on solubility

Solubility of 1-(4-fluorophenyl)-2-(morpholinomethyl)hex-5-yn-1-one

This compound, known as 1-(4-fluorophenyl)-2-(morpholinomethyl)hex-5-yn-1-one, exhibits interesting solubility characteristics that are influenced by its distinct molecular structure. Here are some key points regarding its solubility:

  • Polarity: The presence of the morpholine group contributes to some polarity, making this compound potentially soluble in polar solvents such as water and alcohols.
  • Hydrophobic Effects: The hex-5-yn-1-one structure introduces a hydrophobic region, which may limit solubility in highly polar solvents.
  • Solvents: This compound may be more soluble in organic solvents such as DMSO or ethanol due to its interplay of polar and nonpolar characteristics.
  • pH Dependency: The solubility might also be influenced by the pH of the solution, particularly if it can participate in protonation or deprotonation reactions.

For practical applications, it is essential to consider these factors when assessing the solubility of 1-(4-fluorophenyl)-2-(morpholinomethyl)hex-5-yn-1-one for drug formulation or laboratory settings. The balance between its polar and nonpolar attributes defines how it interacts with various solvents.

Interesting facts

Interesting Facts about 1-(4-fluorophenyl)-2-(morpholinomethyl)hex-5-yn-1-one

1-(4-fluorophenyl)-2-(morpholinomethyl)hex-5-yn-1-one is an intriguing organic compound that demonstrates the intersection of medicinal chemistry and synthetic organic chemistry. Below are some fascinating aspects of this compound:

  • Structural Complexity: This compound features a unique combination of functional groups, including a fluorophenyl moiety and a morpholinomethyl substituent. Such structural diversity allows for exploration in various chemical reactions and potential biological activities.
  • Fluorine Influence: The presence of the fluorine atom in the aromatic ring can significantly enhance the compound’s lipophilicity and metabolic stability, making it a valuable candidate in drug development. Fluorinated compounds often exhibit altered physical and chemical properties, contributing to their efficacy in pharmaceuticals.
  • Potential Biological Activity: Research has shown that compounds with similar structures can exhibit a wide range of biological activities, including anti-cancer, anti-inflammatory, and antimicrobial properties. The exploration of this specific compound could reveal new therapeutic applications.
  • Synthetic Pathways: The synthesis of this compound likely involves multi-step reactions, showcasing the creativity and precision required in organic synthesis. Understanding these pathways helps in refining synthetic techniques to improve yield and reduce by-products.
  • Role in Drug Discovery: Compounds like 1-(4-fluorophenyl)-2-(morpholinomethyl)hex-5-yn-1-one play an essential role in lead optimization during drug discovery, where structural modifications are made to improve potency and selectivity against biological targets.

As research progresses, the insights gained from the study of such compounds continue to illuminate the intricate relationship between molecular structure and biological function, emphasizing the importance of chemistry in innovation and discovery.