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Myosmine chloride

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Identification
Molecular formula
C14H23ClN2O4
CAS number
51-95-0
IUPAC name
[(8R)-3,4,5,6,7,8-hexahydropyrrolizin-4-ium-1-yl]methyl (2R)-2-hydroxy-2-[(1S)-1-hydroxyethyl]-3-methyl-butanoate;chloride
State
State

At room temperature, Myosmine chloride is typically found in a solid state.

Melting point (Celsius)
141.00
Melting point (Kelvin)
414.15
Boiling point (Celsius)
210.00
Boiling point (Kelvin)
483.15
General information
Molecular weight
300.82g/mol
Molar mass
300.8240g/mol
Density
1.2000g/cm3
Appearence

Myosmine chloride appears as a whitish crystalline solid. Its appearance can vary slightly with the form it is in or any impurities present.

Comment on solubility

Solubility of [(8R)-3,4,5,6,7,8-hexahydropyrrolizin-4-ium-1-yl]methyl (2R)-2-hydroxy-2-[(1S)-1-hydroxyethyl]-3-methyl-butanoate;chloride

This compound exhibits a complex solubility profile, influenced by its unique structure and ionic characteristics. It is important to consider the following factors when assessing its solubility:

  • Polarity: The presence of hydroxyl groups contributes to the compound's polarity, which typically enhances solubility in polar solvents, such as water and alcohols.
  • Ionic Nature: As a chloride salt, the presence of a chloride ion may help improve solubility in aqueous solutions due to ion-dipole interactions.
  • Hydrogen Bonding: The hydroxyl groups can engage in hydrogen bonding, facilitating solvation and potentially increasing solubility in polar solvents.
  • Temperature Effects: Solubility may vary with temperature; generally, higher temperatures can lead to increased solubility in many cases.

Due to these complexities, it is vital to conduct empirical solubility studies to understand the compound's behavior in various solvents and conditions. This nuanced approach is often required to predict how such a compound will interact in different environments.

Interesting facts

Interesting Facts About [(8R)-3,4,5,6,7,8-hexahydropyrrolizin-4-ium-1-yl]methyl (2R)-2-hydroxy-2-[(1S)-1-hydroxyethyl]-3-methyl-butanoate;chloride

This unique compound presents a fascinating case study in organic and pharmaceutical chemistry due to its complex structure and potential applications. Here are some noteworthy aspects:

  • Chiral Centers: This compound features multiple chiral centers, which can lead to the existence of different isomers. Understanding these isomers is crucial, as they may exhibit significantly different biological activities.
  • Biological Relevance: Compounds like this one often play important roles in medicinal chemistry, particularly in drug design and development. Investigating its interactions within biological systems can unveil potential therapeutic properties.
  • Structural Complexity: The hexahydropyrrolizin framework introduces a unique cyclic structure that can affect the compound's chemical reactivity and properties. The presence of the pyrrolidine ring often facilitates various chemical reactions, making it a key subject in synthetic organic chemistry.
  • Application Potential: Due to its intricate arrangement of functional groups, this compound may find applications in fields such as agrochemicals, nutraceuticals, or as a precursor in synthetic pathways for more complex molecules.
  • Research Interest: Scientists continually explore similar compounds to elucidate mechanisms of action in biological systems. The study of such compounds can lead to novel drugs or provide insights into metabolic pathways.

In summary, this compound highlights the beauty of chemical diversity and the potential applications that arise from such structures. The exploration of its properties, both physical and biological, can offer exciting avenues for future research and development.

Synonyms
Cyanustine
Cynaustine
(+)-Cyanustine
[(8R)-3,4,5,6,7,8-hexahydropyrrolizin-4-ium-1-yl]methyl (2R)-2-hydroxy-2-[(1S)-1-hydroxyethyl]-3-methylbutanoate;chloride
17958-39-3
orb1991271
AKOS040735532
Butanoic acid, 2,3-dihydroxy-2-(1-methylethyl)-, (2,3,5,7a-tetrahydro-1H-pyrrolizin-7-yl)methyl ester, (7aR-(7(2S*,3S*),7aR*))-