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3-morpholino-1,1-bis(3-thienyl)butan-1-ol

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Identification
Molecular formula
C17H21NO2S2
CAS number
155205-09-9
IUPAC name
3-morpholino-1,1-bis(3-thienyl)butan-1-ol
State
State

At room temperature, the compound is generally in a solid state, primarily appearing as a stable crystalline powder.

Melting point (Celsius)
95.00
Melting point (Kelvin)
368.15
Boiling point (Celsius)
507.00
Boiling point (Kelvin)
780.15
General information
Molecular weight
321.44g/mol
Molar mass
321.4360g/mol
Density
1.2300g/cm3
Appearence

3-Morpholino-1,1-bis(3-thienyl)butan-1-ol appears as a white to off-white crystalline powder. The compound is typically characterized by its solid form and fine particulate nature when synthesized and stored appropriately.

Comment on solubility

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

The solubility of 3-morpholino-1,1-bis(3-thienyl)butan-1-ol can be characterized by several important factors:

  • Polar and Non-Polar Interactions: This compound contains both a morpholino group and thienyl groups, which can impact its solubility in different solvents. The morpholino group is polar, which suggests increased solubility in polar solvents such as water.
  • Hydroxyl Group Influence: The presence of the -OH (hydroxyl) group typically enhances solubility in polar solvents due to hydrogen bonding.
  • Thienyl Contribution: The thienyl groups, being aromatic, may contribute some hydrophobic characteristics, potentially limiting solubility in extremely polar solvents.

Based on these structural features, one might anticipate the following solubility behaviors:

  1. Good solubility in alcohols and ethers where hydrogen bonding can occur.
  2. Moderate solubility in water, possibly aided by the hydroxyl group's ability to interact with water molecules.
  3. Poor solubility in highly non-polar solvents due to the hydrophobic thienyl groups.

In practical applications, these solubility characteristics are crucial to consider for formulation and synthesis processes, as they can influence the compound's reactivity and efficacy.

Interesting facts

Interesting Facts about 3-Morpholino-1,1-bis(3-thienyl)butan-1-ol

3-Morpholino-1,1-bis(3-thienyl)butan-1-ol is a fascinating compound that belongs to a category of organic molecules which often exhibit remarkable biological and chemical properties. Here are some intriguing aspects of this compound:

  • Pharmacological Potential: Due to the presence of the morpholine ring, this compound has garnered interest for its potential pharmaceutical applications. Morpholine derivatives are known for their diverse biological activities, which can include antitumor, anti-inflammatory, and antibacterial properties.
  • Thienyl Groups: The incorporation of thienyl groups not only provides unique electronic properties but also enhances the molecule's ability to participate in various chemical reactions. These sulfur-containing rings can lend the compound interesting redox properties, which could be useful in materials science and organic electronics.
  • Synthetic Versatility: The synthesis of compounds like 3-morpholino-1,1-bis(3-thienyl)butan-1-ol typically involves multi-step processes that may include reactions such as nucleophilic substitutions and coupling reactions. This opens up avenues for chemists to explore modifications that could yield derivatives with improved characteristics.
  • Research Applications: Compounds of similar structure have been studied for their potential roles in medicinal chemistry, particularly in drug design. Insights gained from studying such compounds may lead to the development of new therapeutics targeting various diseases.
  • Mechanistic Studies: The complexity of this compound offers chemists a rich platform for exploring reaction mechanisms. Understanding how it behaves in different environments can reveal fundamental insights into both organic chemistry and material science.

In summary, 3-morpholino-1,1-bis(3-thienyl)butan-1-ol presents a unique structure that combines pharmacological promise with interesting chemical properties. Its study not only contributes to our understanding of complex organic molecules but also highlights the interdisciplinary connections between chemistry, biology, and materials science.