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Diethylpropion

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Identification
Molecular formula
C18H25NO2S2
CAS number
18778-73-1
IUPAC name
3-(diethylamino)-1,1-bis(3-thienyl)butan-1-ol
State
State

At room temperature, Diethylpropion is in a solid state. It is stable and can be stored under standard conditions without significant degradation. The solid nature contributes to its manipulability during analytical and synthetic procedures.

Melting point (Celsius)
98.00
Melting point (Kelvin)
371.15
Boiling point (Celsius)
281.00
Boiling point (Kelvin)
554.15
General information
Molecular weight
321.49g/mol
Molar mass
321.4940g/mol
Density
1.1588g/cm3
Appearence

Diethylpropion typically appears as a white, crystalline powder. This compound is known for its aesthetic purity and smooth texture. The crystals can be observed under magnification, showcasing uniform and intricate shapes typical of crystalline substances.

Comment on solubility

Solubility of 3-(diethylamino)-1,1-bis(3-thienyl)butan-1-ol

The solubility of 3-(diethylamino)-1,1-bis(3-thienyl)butan-1-ol is influenced by several key factors, primarily due to its unique chemical structure. This compound exhibits both polar and nonpolar characteristics, owing to the presence of the diethylamino group as well as the thienyl rings.

When considering its solubility:

  • Polar Solvents: Compounds with an amino group tend to be more soluble in polar solvents like water or alcohols due to hydrogen bonding.
  • Nonpolar Solvents: The thienyl moieties contribute to some hydrophobic character, potentially enhancing solubility in nonpolar solvents like hexane or toluene.
  • Mixed Solvent Systems: In cases where mixed solvents are utilized, the compound might show varying levels of solubility depending on the ratios used.

Furthermore, it is important to consider the following factors:

  1. Temperature: Higher temperatures typically increase solubility for most organic compounds.
  2. pH Levels: The solubility may also vary with changes in pH, particularly since the compound contains an amino group that can undergo protonation or deprotonation.
  3. Concentration: In saturated solutions, interactions between molecules may affect overall solubility limits.

In conclusion, while this compound may exhibit reasonable solubility in both polar and nonpolar environments due to its versatile structure, empirical testing remains the most reliable method to determine its exact solubility characteristics under varying conditions. As the saying goes, *“The devil is in the details”* – a closer examination of these factors will reveal the true solubility behavior of 3-(diethylamino)-1,1-bis(3-thienyl)butan-1-ol.

Interesting facts

Exploring 3-(Diethylamino)-1,1-bis(3-thienyl)butan-1-ol

This compound, commonly known in the field of organic chemistry, exhibits unique characteristics that have captured the attention of scientists and chemists. It is particularly notable for its intriguing structural features and potential applications.

Key Features

  • Diverse Applications: This compound can be used in various fields, including pharmaceuticals, where its unique structure may contribute to biological activity.
  • Structural Significance: The presence of thienyl groups in its structure offers valuable insights into the properties of sulfur-containing heterocycles, which are a significant class of compounds in medicinal chemistry.
  • Intriguing Chemistry: The diethylamino group introduces basic properties that may influence the compound's reactivity and solubility, providing a rich area for exploration in synthetic organic chemistry.
  • Potential for Innovation: Compounds like this can act as building blocks in the development of more complex molecules, paving the way for innovations in drug design and materials science.

As highlighted by chemists, “The creative combination of different functional groups can lead to unexpected properties and functionalities.” Studying this compound not only enhances our understanding of complex organic molecules but also opens doors to new research avenues.

In conclusion, 3-(diethylamino)-1,1-bis(3-thienyl)butan-1-ol serves as a prime example of the intricate beauty of organic chemistry, encouraging continuous exploration and innovation within the scientific community. With its multifaceted applications and structural intrigue, it exemplifies the dynamic nature of chemical research.