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Ethylstyryl ketone

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Identification
Molecular formula
C20H23NO
CAS number
3908-84-1
IUPAC name
1-(diethylamino)-4,4-diphenyl-but-3-en-2-one
State
State

At room temperature, 1-(diethylamino)-4,4-diphenyl-but-3-en-2-one is in a solid state. It is stable under ordinary conditions and does not readily sublimate or evaporate.

Melting point (Celsius)
80.00
Melting point (Kelvin)
353.20
Boiling point (Celsius)
375.50
Boiling point (Kelvin)
648.70
General information
Molecular weight
293.41g/mol
Molar mass
293.4110g/mol
Density
1.0700g/cm3
Appearence

1-(Diethylamino)-4,4-diphenyl-but-3-en-2-one typically appears as a white to off-white crystalline solid. It may also be encountered in a powdered form depending on the preparation and handling conditions.

Comment on solubility

Solubility of 1-(diethylamino)-4,4-diphenyl-but-3-en-2-one

1-(diethylamino)-4,4-diphenyl-but-3-en-2-one is known for its unique structure, which can influence its solubility properties. When considering the solubility of this compound, several factors come into play:

  • Polarity: The presence of the diethylamino group adds to the polarity of the molecule, which may enhance the solubility in polar solvents like water and alcohols.
  • Hydrophobic Regions: With multiple phenyl groups in its structure, this compound also possesses hydrophobic characteristics that could limit its solubility in polar solvents.
  • Solvent Choice: It is likely to be more soluble in organic solvents such as chloroform, ether, or acetone due to the non-polar phenyl rings.
  • Temperature: Temperature may also play a critical role, as increased heat often enhances solubility for organic compounds.

In summary, while 1-(diethylamino)-4,4-diphenyl-but-3-en-2-one may exhibit reasonable solubility in both polar and non-polar solvents depending on the conditions, it is primarily more soluble in organic solvents. As always, empirical solubility testing is recommended to confirm the predictions based on theoretical considerations.

Interesting facts

Interesting Facts About 1-(diethylamino)-4,4-diphenyl-but-3-en-2-one

1-(diethylamino)-4,4-diphenyl-but-3-en-2-one, often referred to in the context of its applications in medicinal chemistry and organic synthesis, is a noteworthy compound with a variety of intriguing characteristics. This compound is a member of the class of enones, which play significant roles in various chemical reactions.

  • Diverse Applications: It is utilized as an intermediate in the synthesis of pharmaceuticals and other organic compounds. The unique structure allows for modifications that lead to diverse biological activities.
  • Biological Activity: Compounds similar to 1-(diethylamino)-4,4-diphenyl-but-3-en-2-one often exhibit a range of pharmacological effects. Research into its derivatives can reveal potential medicinal properties, including anti-inflammatory and anti-cancer activities.
  • Mechanistic Insights: The presence of the diethylamino group enhances nucleophilicity, making this compound a valuable participant in various nucleophilic substitution reactions.
  • Research Potential: With ongoing studies into the structure-activity relationship (SAR) of related compounds, this particular chemical can provide insights into design strategies for new therapeutic agents.

Moreover, the phenomenon of photoisomerization in such enones is of particular interest to researchers, as exposure to UV light can induce structural changes that might be useful in developing light-sensitive materials or drug delivery systems. The versatility of this compound illustrates the intricate connections between chemistry and biology, highlighting the importance of ongoing research in discovering and refining new pharmaceuticals. As the landscape of medicinal chemistry evolves, compounds like 1-(diethylamino)-4,4-diphenyl-but-3-en-2-one remain at the forefront, showcasing the dynamic nature of chemical exploration.

Synonyms
BRN 2809400
3-BUTEN-2-ONE, 1-(DIETHYLAMINO)-4,4-DIPHENYL-
1-(Diethylamino)-4,4-diphenyl-3-buten-2-one
1866-44-0
DTXSID40171920
DTXCID8094411