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Vincristine

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Identification
Molecular formula
C46H56N4O10
CAS number
57-22-7
IUPAC name
1-[(4S)-14-hydroxy-15-oxa-1,11-diazahexacyclo[16.3.1.04,12.04,21.05,10.013,19]docosa-5,7,9,17-tetraen-11-yl]ethanone
State
State

Vincristine is a solid at room temperature, typically available in a crystalline powder form for pharmaceutical use.

Melting point (Celsius)
267.00
Melting point (Kelvin)
540.15
Boiling point (Celsius)
-1.00
Boiling point (Kelvin)
-1.00
General information
Molecular weight
824.98g/mol
Molar mass
824.9830g/mol
Density
1.4500g/cm3
Appearence

Vincristine appears as a white to off-white crystalline powder. It is typically odorless and sensitive to light.

Comment on solubility

Solubility Considerations

The compound 1-[(4S)-14-hydroxy-15-oxa-1,11-diazahexacyclo[16.3.1.04,12.04,21.05,10.013,19]docosa-5,7,9,17-tetraen-11-yl]ethanone is quite intriguing in terms of solubility due to its complex molecular structure. Generally speaking, the solubility of a compound is primarily influenced by factors such as:

  • Molecular Structure: The presence of functional groups, like hydroxyl groups, can enhance solubility in polar solvents.
  • Polarity: Highly polar compounds tend to dissolve better in polar solvents (like water) while non-polar compounds are more soluble in non-polar solvents.
  • Hydrogen Bonding: Molecules capable of forming hydrogen bonds, such as those containing -OH or -NH groups, typically exhibit increased solubility in water.
  • Large Aromatic Systems: The extensive aromatic framework present in this compound might increase its hydrophobic character, which can decrease solubility in polar solvents.

For 1-[(4S)-14-hydroxy-15-oxa-1,11-diazahexacyclo[16.3.1.04,12.04,21.05,10.013,19]docosa-5,7,9,17-tetraen-11-yl]ethanone, it is essential to note that its solubility could vary significantly depending on the solvent used. In summary, while the compound may be partially soluble in polar solvents due to its hydroxyl group, the overall solubility is likely limited by the bulky hydrophobic regions of the molecule. As with many complex organic compounds, understanding its solubility profile could require empirical testing to draw definitive conclusions.

Interesting facts

Interesting Facts about 1-[(4S)-14-hydroxy-15-oxa-1,11-diazahexacyclo[16.3.1.04,12.04,21.05,10.013,19]docosa-5,7,9,17-tetraen-11-yl]ethanone

This compound is a remarkable member of the class of organic molecules known for their intricate structures and potential applications. Here are some engaging insights regarding this fascinating compound:

  • Complex Structure: The compound is characterized by a unique hexacyclic framework, indicating a high level of molecular complexity. This structural intricacy often results in intriguing chemical properties.
  • Biological Significance: Compounds similar to this chemical are often studied for their roles in biological systems. Many such molecules exhibit significant pharmacological activities, which makes them valuable in medicinal chemistry.
  • Synthetic Interest: The synthesis of this compound may involve advanced organic chemistry techniques. The creation of such complex molecules is a challenge that can lead to new methodologies being developed in the field.
  • Potential Applications: Compounds with such unique structures may have potential applications ranging from drug design to materials science. Their ability to interact with biological targets may lead to the discovery of novel therapeutic agents.
  • Research Frontiers: Ongoing research is likely to explore the detailed mechanisms of action, potential therapeutic uses, and the synthesis routes of this compound, thereby enriching the scientific literature.

As research on compounds like 1-[(4S)-14-hydroxy-15-oxa-1,11-diazahexacyclo[16.3.1.04,12.04,21.05,10.013,19]docosa-5,7,9,17-tetraen-11-yl]ethanone continues, scientists remain excited about their potential to revolutionize various fields, including pharmacology and materials science. This compound serves as a prime example of how intricate chemistry can lead to groundbreaking discoveries.