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AH-7921

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Identification
Molecular formula
C23H29NOS2
CAS number
55154-30-8
IUPAC name
3-(1-piperidyl)-1,1-bis(3-thienyl)butan-1-ol
State
State

At room temperature, AH-7921 is a solid. It is typically handled in powder form.

Melting point (Celsius)
212.00
Melting point (Kelvin)
485.15
Boiling point (Celsius)
375.00
Boiling point (Kelvin)
648.15
General information
Molecular weight
353.52g/mol
Molar mass
353.5190g/mol
Density
1.2234g/cm3
Appearence

AH-7921 appears as a powder or crystalline solid. It is typically white or off-white in color.

Comment on solubility

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

The solubility of 3-(1-piperidyl)-1,1-bis(3-thienyl)butan-1-ol is a topic of interest due to its unique structure and interactions. This compound's solubility can be influenced by various factors, such as:

  • Polarity: The presence of polar functional groups like the alcohol moiety tends to enhance solubility in polar solvents like water.
  • Hydrogen Bonding: The hydroxyl group can form hydrogen bonds, which facilitates solvation in aqueous environments.
  • Hydrophobic Interactions: The thienyl rings contribute hydrophobic characteristics, potentially lowering solubility in polar solvents.
  • Steric Effects: The bulky piperidyl group may affect how well the compound can interact with solvent molecules.

In a more general context, it can be said that:

  1. Compounds with multiple polar functional groups often show increased solubility in water.
  2. Hydrophobic regions can lead to decreased solubility in polar solvents but may enhance solubility in organic solvents.
  3. Temperature can also play a critical role, as increased temperature typically enhances solubility.

In summary, while we can predict certain solubility trends based on the molecular structure of 3-(1-piperidyl)-1,1-bis(3-thienyl)butan-1-ol, empirical testing in various solvents is necessary to establish its exact solubility profiles. Understanding the balance between the polar and non-polar characteristics of this compound is key to predicting its behavior in different solutions.

Interesting facts

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

3-(1-piperidyl)-1,1-bis(3-thienyl)butan-1-ol is a fascinating compound that embodies unique structural characteristics and potential applications in the realm of medicinal chemistry. This compound features a complex arrangement that includes:

  • Thienyl Groups: The presence of two thienyl rings provides the molecule with distinct chemical reactivity and potential electronic properties.
  • Piperidine Ring: The incorporation of a piperidyl moiety can influence the compound's pharmacological activity, often enhancing its interaction with biological targets.
  • Alcohol Functional Group: The -OH group on the butan-1-ol portion plays a vital role in solubility and reactivity, making it an essential feature for potential drug formulations.

This compound exemplifies how intricate molecular designs can lead to valuable pharmacological properties. It is noteworthy for its potential influences on:

  • Neuropharmacology: Given its piperidine and thienyl components, it has been investigated for efficacy in neurological conditions.
  • Antimicrobial Activity: Compounds containing thienyl moieties often display interesting antimicrobial properties, highlighting the importance of researching their biological interactions.
  • Structure-Activity Relationships (SAR): The novel structure opens doors to studying how variations in the molecular framework can affect biological function.

The research surrounding 3-(1-piperidyl)-1,1-bis(3-thienyl)butan-1-ol continues to evolve, demonstrating the significance of understanding its comprehensive properties. As scientists investigate its potential, phrases like "the marriage of structure and activity" ring true in the quest for innovative therapeutic solutions.


Overall, this compound serves as a compelling example of the intricate relationship between chemical structure and biological activity, encouraging further exploration in the fields of organic chemistry and pharmacology.