Thiobutobenzone | Solubility of Things

Identification

Molecular formula

C₁₈H₁₉NO₂S

CAS number

1420-50-0

IUPAC name

1-morpholino-4-phenyl-4-(2-thienyl)but-3-en-2-one

State

Thiobutobenzone is a solid at room temperature, usually found in its crystalline form.

Melting point (Celsius)

119.00

Melting point (Kelvin)

392.15

Boiling point (Celsius)

429.15

Boiling point (Kelvin)

702.30

General information

Molecular weight

309.40g/mol

Molar mass

309.3980g/mol

Density

1.2130g/cm³

Appearence

Thiobutobenzone appears as a crystalline solid with a distinct crystalline form. It is typically off-white to beige in color.

Comment on solubility

Solubility of 1-Morpholino-4-phenyl-4-(2-thienyl)but-3-en-2-one

The solubility behavior of 1-morpholino-4-phenyl-4-(2-thienyl)but-3-en-2-one is a topic of interest for both its practical applications and theoretical implications. This compound, characterized by its unique structure, showcases solubility that can be influenced by various factors.

Key Points on Solubility:

Solubility in Organic Solvents: This compound is likely to exhibit good solubility in organic solvents such as dichloromethane, ethanol, and acetone due to its non-polar thienyl and phenyl groups, which enhance its interaction with similar solvent molecules.
Solubility in Water: Water solubility might be limited because of the presence of the hydrophobic regions of the molecule, thus suggesting that the compound would prefer to dissolve in organic rather than aqueous environments.
Temperature Effects: Like many organic compounds, the solubility of 1-morpholino-4-phenyl-4-(2-thienyl)but-3-en-2-one could increase with temperature, which is particularly relevant for applications requiring high dissolution rates.

In summary, while 1-morpholino-4-phenyl-4-(2-thienyl)but-3-en-2-one is more soluble in non-polar solvents, one should always consider the specific application context when evaluating its solubility characteristics. As with many organic compounds, the intricate balance of polarity and molecular interactions plays a crucial role in defining its solubility landscape.

Interesting facts

Interesting Facts about 1-Morpholino-4-phenyl-4-(2-thienyl)but-3-en-2-one

1-Morpholino-4-phenyl-4-(2-thienyl)but-3-en-2-one is a fascinating compound notable for its unique structural characteristics and potential applications in various fields. Here are some intriguing insights about this compound:

Morpholine Ring: The presence of the morpholine ring plays a significant role in enhancing the compound's pharmacological properties. Morpholine derivatives are often known for their ability to interact with biological targets, making them valuable in medicinal chemistry.
Thienyl Group: The incorporation of a thienyl group introduces additional polarity and electronic properties. Thiophene and its derivatives have been extensively studied for their role in organic semiconductors and photovoltaic cells.
Alkenone Framework: The structural framework includes a conjugated alkenone system, which contributes to the compound's stability and reactivity. Substituents on this framework can influence both physical and chemical properties, making it an important area of study for synthetic chemists.
Potential Applications: This compound holds promise in the development of new pharmaceuticals, particularly in areas targeting cancer treatment and anti-inflammatory activity. The multifunctional nature of its structure allows for modified derivatives that could potentially enhance efficacy.

In the words of renowned chemist Robert H. Grubbs, who once said, "The beauty of chemistry lies in its ability to create new molecules with intricate design and profound implications." This quote resonates well with the exploration of compounds like 1-morpholino-4-phenyl-4-(2-thienyl)but-3-en-2-one, as each modification can lead to remarkable advancements in chemistry and medicine.

In summary, 1-morpholino-4-phenyl-4-(2-thienyl)but-3-en-2-one exemplifies the beauty and complexity of synthetic organic chemistry, showcasing the interplay of structure and function in chemical compounds.