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Monensin A

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Identification
Molecular formula
C36H62O11
CAS number
17090-79-8
IUPAC name
9-(1-hydroxyethyl)-3-[4-(3-hydroxyphenyl)-4-methoxy-1-methyl-butyl]-4,14,16,16-tetramethyl-2,6,10,17-tetraoxatricyclo[11.3.1.11,5]octadec-13-ene-7,11-dione
State
State

Monensin A is generally a solid at room temperature, presenting itself as a crystalline powder. Its limited solubility in water corroborates its solid state.

Melting point (Celsius)
268.00
Melting point (Kelvin)
541.00
Boiling point (Celsius)
448.00
Boiling point (Kelvin)
721.00
General information
Molecular weight
670.89g/mol
Molar mass
670.8890g/mol
Density
1.2300g/cm3
Appearence

Monensin A is a white to off-white crystalline solid. It is typically encountered as a powder or a solid block. The compound is quite insoluble in water, contributing to its solid state appearance under standard conditions.

Comment on solubility

Solubility of 9-(1-hydroxyethyl)-3-[4-(3-hydroxyphenyl)-4-methoxy-1-methyl-butyl]-4,14,16,16-tetramethyl-2,6,10,17-tetraoxatricyclo[11.3.1.11,5]octadec-13-ene-7,11-dione (C36H62O11)

The solubility of this complex compound is influenced by its intricate molecular structure and the presence of various functional groups. When examining the solubility characteristics, it is essential to consider the following aspects:

  • Polarity: The numerous hydroxyl (–OH) groups present in the compound generally enhance solubility in polar solvents, while the large hydrophobic portions could lead to reduced solubility in nonpolar solvents.
  • Hydrogen Bonding: Compounds with multiple –OH groups can participate in hydrogen bonding, which can significantly affect solubility in water. This is particularly true for substances exhibiting high hydrogen-bonding capabilities.
  • Solvent Interaction: This molecule may demonstrate varied solubility in different organic solvents. For instance, it might show good solubility in ethanol or methanol due to its polar characteristics, while it may be poorly soluble in hydrocarbons.
  • Temperature Dependency: Like many organic compounds, the solubility may change with temperature; as temperature increases, solubility in many solvents often increases.

In summary, while the presence of multiple functional groups like hydroxyls can enhance solubility in polar solvents, the overall hydrophobic nature of the compound's structure may lead to challenges in solubility, especially in nonpolar environments. Understanding these factors is crucial when predicting how this compound interacts with various solvents.

Interesting facts

Interesting Facts about 9-(1-Hydroxyethyl)-3-[4-(3-hydroxyphenyl)-4-methoxy-1-methyl-butyl]-4,14,16,16-tetramethyl-2,6,10,17-tetraoxatricyclo[11.3.1.11,5]octadec-13-ene-7,11-dione

This compound, known for its intricate structure, is a fascinating example of the complexity associated with organic molecules. It features a unique combination of functional groups that opens up a realm of potential applications in chemistry and other fields. Here are some intriguing highlights about this compound:

  • Structural Complexity: The compound showcases a multi-ring structure and incorporates multiple hydroxy and methoxy groups, which are significant for influencing its chemical reactivity and interactions.
  • Potential Applications: Compounds of this nature are often explored for their therapeutic potential, particularly in pharmacology. They may possess bioactive properties due to their phenolic and dione functionalities.
  • Mechanistic Insights: Understanding the reactivity of 9-(1-hydroxyethyl)-3-[4-(3-hydroxyphenyl)-4-methoxy-1-methyl-butyl]-4,14,16,16-tetramethyl-2,6,10,17-tetraoxatricyclo[11.3.1.11,5]octadec-13-ene-7,11-dione can provide insights into reaction mechanisms that are valuable in synthetic chemistry.
  • Research Significance: The study of such complex organic compounds contributes to the broader understanding of organic synthesis and mechanism, paving the way toward innovative materials and drugs.

The combination of various substituents and ring structures makes the compound not only a subject of academic interest but also a potential player in the development of new pharmaceuticals, possibly enhancing efficacy or reducing side effects in therapeutic contexts. Research into this class of compounds fuels advances in medicinal chemistry and offers hope for new treatments in various medical fields.

Synonyms
Anhydrodebromoaplysiatoxin
63543-22-6
Aplysiatoxin, 17-debromo-3,4-didehydro-3-deoxy-
(1S,3R,4S,5S,9R)-9-((1R)-1-hydroxyethyl)-3-((2S,5S)-5-(3-hydroxyphenyl)-5-methoxypentan-2-yl)-4,14,16,16-tetramethyl-2,6,10,17-tetraoxatricyclo(11.3.1.11,5)octadec-13-ene-7,11-dione
(1S,3R,4S,5S,9R)-9-[(1R)-1-hydroxyethyl]-3-[(2S,5S)-5-(3-hydroxyphenyl)-5-methoxypentan-2-yl]-4,14,16,16-tetramethyl-2,6,10,17-tetraoxatricyclo[11.3.1.11,5]octadec-13-ene-7,11-dione
DTXSID501335140
9-(1-hydroxyethyl)-3-(5-(3-hydroxyphenyl)-5-methoxypentan-2-yl)-4,14,16,16-tetramethyl-2,6,10,17-tetraoxatricyclo(11.3.1.11,5)octadec-13-ene-7,11-dione