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Identification
Molecular formula
C15H19NOS
CAS number
69492-51-9
IUPAC name
4-(diethylamino)-3,4-dihydro-2H-1-benzothiepin-5-one
State
State

At room temperature, 4-(diethylamino)-3,4-dihydro-2H-1-benzothiepin-5-one is typically found in a solid state.

Melting point (Celsius)
102.00
Melting point (Kelvin)
375.15
Boiling point (Celsius)
300.00
Boiling point (Kelvin)
573.00
General information
Molecular weight
261.38g/mol
Molar mass
261.3840g/mol
Density
1.1900g/cm3
Appearence

The compound 4-(diethylamino)-3,4-dihydro-2H-1-benzothiepin-5-one appears as a crystalline solid. It is characterized by a solid structure that is typically colorless to pale yellow.

Comment on solubility

Solubility Characteristics of 4-(diethylamino)-3,4-dihydro-2H-1-benzothiepin-5-one

The solubility of 4-(diethylamino)-3,4-dihydro-2H-1-benzothiepin-5-one can be quite complex due to its unique structure. Understanding the solubility profile of this compound is essential for various applications, and several factors come into play:

  • Polarity: The presence of the diethylamino group increases the overall polarity of the molecule, potentially enhancing its solubility in polar solvents.
  • Solvent Compatibility: It is likely to be soluble in organic solvents such as ethanol, methanol, and dichloromethane due to the hydrophobic aromatic ring.
  • pH Sensitivity: The solubility might vary depending on the pH of the solution, as protonation of the amino group can lead to higher solubility in aqueous environments.
  • Temperature Effects: Increased temperature may also improve solubility, which is a common phenomenon for many organic compounds.

In summary, while 4-(diethylamino)-3,4-dihydro-2H-1-benzothiepin-5-one shows potential for solubility in various solvents, its behavior is a function of temperature, polarity, and chemical environment. Further experimental insights would greatly aid in fully characterizing its solubility properties.

Interesting facts

Interesting Facts about 4-(Diethylamino)-3,4-dihydro-2H-1-benzothiepin-5-one

This intriguing compound is a member of the benzothiepin class, which features a fused ring structure containing both a thiophene and a phenyl group. Its unique chemical structure has led researchers to explore its potential applications in various fields, particularly in pharmacology.

Notable Aspects:

  • Potential Pharmacological Applications: The diethylamino group on this compound may enhance its biological activity, making it a candidate for further study as a pharmaceutical agent.
  • Structural Significance: The presence of the benzothiepin moiety is crucial, as compounds containing this structure have demonstrated interesting neuropharmacological properties.
  • Research Interest: The compound has garnered attention for its potential role in treating disorders that may involve dopaminergic pathways, given the relevance of its structure to known dopamine receptor ligands.
  • Versatility in Synthesis: Chemists have developed various synthetic routes to produce benzothiepin derivatives, which allows for the exploration of different substituents on the core structure, influencing the compound's biological activities.

Furthermore, studies investigating benzothiepin derivatives like this compound have resulted in discoveries of novel compounds that exhibit remarkable therapeutic benefits. As research continues, our understanding of how structural modifications can impact biological effects will likely pave the way for new medicinal innovations.

In summary, 4-(diethylamino)-3,4-dihydro-2H-1-benzothiepin-5-one exemplifies the interplay between organic chemistry and pharmacology, showcasing how the tiniest changes in molecular structure can lead to significant biological implications.