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Hymenoxin

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Identification
Molecular formula
C16H22NO5
CAS number
313-84-6
IUPAC name
(7-hydroxy-5,6,7,8-tetrahydro-3H-pyrrolizin-1-yl)methyl 2-hydroxy-2-isopropyl-3-methoxy-butanoate
State
State

At room temperature, hymenoxin exists in a solid state, often in the form of crystalline powder.

Melting point (Celsius)
150.50
Melting point (Kelvin)
423.70
Boiling point (Celsius)
361.25
Boiling point (Kelvin)
634.40
General information
Molecular weight
302.37g/mol
Molar mass
302.3650g/mol
Density
1.1700g/cm3
Appearence

Hymenoxin is a white to off-white crystalline powder. It is relatively non-volatile under standard conditions.

Comment on solubility

Solubility of (7-hydroxy-5,6,7,8-tetrahydro-3H-pyrrolizin-1-yl)methyl 2-hydroxy-2-isopropyl-3-methoxy-butanoate

The solubility of (7-hydroxy-5,6,7,8-tetrahydro-3H-pyrrolizin-1-yl)methyl 2-hydroxy-2-isopropyl-3-methoxy-butanoate is influenced by various factors, making it a compound of interest in solubility studies. Here are some key points related to its solubility:

  • Polar vs. Non-Polar: The presence of hydroxyl groups in this compound tends to enhance its solubility in polar solvents, such as water, due to hydrogen bonding.
  • Hydrophobic Characteristics: The alkyl chain contributions from the isopropyl and methoxy groups may impart hydrophobic characteristics, potentially limiting solubility in non-polar solvents.
  • pH Dependence: The solubility may also be pH-dependent. At different pH levels, the ionization of functional groups could create variations in solubility.
  • Temperature Influences: As with many organic compounds, temperature can greatly affect solubility. Generally, higher temperatures increase solubility in most solvents.

Overall, the solubility of this compound can be characterized as quite variable, warranting further experimental analysis to determine its precise solubility profile in various environments. Understanding these solubility parameters is crucial for applications in pharmaceuticals and chemical formulations.

Interesting facts

Exploring the Uniqueness of (7-Hydroxy-5,6,7,8-tetrahydro-3H-pyrrolizin-1-yl)methyl 2-hydroxy-2-isopropyl-3-methoxy-butanoate

This compound, with its intriguing structure, belongs to a remarkable class of organic molecules known for their diverse applications and properties. Here are some fascinating insights about it:

  • Complex Structure: The presence of the pyrrolizin ring system adds a level of complexity to the molecule, which may influence its reactivity and interaction with other compounds.
  • Potential Biological Activity: Compounds with similar frameworks are often explored for their pharmacological potential, including anti-inflammatory and analgesic properties.
  • Chirality in Action: This compound exhibits chirality due to the presence of chiral centers, making it an interesting candidate for studies in stereochemistry and its effects on biological activity.
  • Natural Product Connections: Structures resembling this compound can frequently be found in various natural products, indicating that it could serve as a model for synthetic studies aimed at creating derivatives with enhanced activity.
  • Applications in Organic Synthesis: The functional groups present in this compound can also make it a relevant intermediate in organic synthesis, aiding the formation of more complex molecules.

The exploration of this compound opens doors to numerous avenues in medicinal chemistry, organic synthesis, and stereochemistry, challenging researchers and students alike to unveil its potential. As quoted by a famous chemist, "Every compound has a story to tell." The narrative of this particular molecule is one of complexity, potential, and the endless quest for knowledge in the ever-evolving field of chemistry.

Synonyms
Heliotron
Butanoic acid, 2-hydroxy-2-[(1R)-1-methoxyethyl]-3-methyl-,[(1R,7aR)-2,3,5,7a-tetrahydro-1-hydroxy-1H-pyrrolizin-7-yl]methyl ester,(2S)-
59532-50-2
Oprea1_092322
Oprea1_789858
SCHEMBL893305
LMFKRLGHEKVMNT-UHFFFAOYSA-N
DB-214608
(1-Hydroxy-2,3,5,7a-tetrahydro-1H-pyrrolizin-7-yl)methyl 2-hydroxy-2-isopropyl-3-methoxybutanoate #
(1-Hydroxy-2,3,5,7a-tetrahydro-1H-pyrrolizin-7-yl)methyl 2-hydroxy-3-methoxy-2-(propan-2-yl)butanoate
Butanoic acid, 2-hydroxy-2-(1-methoxyethyl)-3-methyl-, (2,3,5,7a-tetrahydro-1-hydroxy-1H-pyrrolizin-7-yl)methyl ester, [1S-[1.alpha.,7(2R*,3S*),7a.alpha.]]-