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Taxol

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Identification
Molecular formula
C47H51NO14
CAS number
33069-62-4
IUPAC name
methyl 16-methoxy-4,15-dimethyl-3-oxo-28-oxa-4,14,19-triazaoctacyclo[12.11.2.115,18.02,6.07,27.08,13.019,26.020,25]octacosa-1,6,8,10,12,20,22,24,26-nonaene-16-carboxylate
State
State
At room temperature, Taxol is in a solid state in the form of white to off-white crystalline powder. It is typically handled as a solid in its pure form, although it may be dissolved in solutions for applications in pharmaceuticals.
Melting point (Celsius)
213.00
Melting point (Kelvin)
486.10
Boiling point (Celsius)
386.90
Boiling point (Kelvin)
660.00
General information
Molecular weight
854.91g/mol
Molar mass
854.9060g/mol
Density
1.3500g/cm3
Appearence

Taxol appears as a white to off-white crystalline powder. It is a compound that is well known for its usage in cancer treatment, particularly for breast and ovarian cancers. As a solid at room temperature, its appearance is consistent with other crystalline organic compounds.

Comment on solubility

Solubility of Methyl 16-methoxy-4,15-dimethyl-3-oxo-28-oxa-4,14,19-triazaoctacyclo[12.11.2.115,18.02,6.07,27.08,13.019,26.020,25]octacosa-1,6,8,10,12,20,22,24,26-nonaene-16-carboxylate (C47H51NO14)

The solubility of complex organic compounds such as methyl 16-methoxy-4,15-dimethyl-3-oxo-28-oxa-4,14,19-triazaoctacyclo[12.11.2.115,18.02,6.07,27.08,13.019,26.020,25]octacosa-1,6,8,10,12,20,22,24,26-nonaene-16-carboxylate can vary significantly based on several factors. Its solubility characteristics include:

  • Polarity: The presence of functional groups such as the carboxylate can impart both polar characteristics, which may enhance solubility in polar solvents like water.
  • Hydrophobic Regions: The complex structure may have hydrophobic regions that resist solubilization in water, favoring solubility in organic solvents like ethanol or acetone.
  • Temperature: Increased temperatures typically improve solubility, as kinetic energy allows more interactions between solvent and solute.
  • pH Dependency: The ionization state of the carboxylate group can change with pH, potentially enhancing solubility in basic conditions.

In summary, the solubility of this compound is likely influenced by a combination of its molecular structure, the nature of its functional groups, and the solvent's properties. For best results, experimentation with various solvents and conditions is recommended to determine optimal solubility.

Interesting facts

Interesting Facts About Methyl 16-methoxy-4,15-dimethyl-3-oxo-28-oxa-4,14,19-triazaoctacyclo[12.11.2.115,18.02,6.07,27.08,13.019,26.020,25]octacosa-1,6,8,10,12,20,22,24,26-nonaene-16-carboxylate

This fascinating compound is a complex organic molecule known for its intricate structure, which contains multiple functional groups and a rich landscape of fused rings. Here are some intriguing points about this compound:

  • Structural Complexity: The name of the compound suggests a significant degree of complexity, featuring octacyclic arrangements that provide unique properties and potential applications in various fields of chemistry.
  • Diversity in Functional Groups: The presence of methoxy and carboxylate groups in its structure implies potential reactivity that can be useful in synthetic chemistry, allowing for numerous derivatives to be explored.
  • Biological Relevance: Compounds with similar structural motifs are often investigated for their biological activity, making this compound a candidate for potential pharmacological applications. The unique scaffold may interact with biological targets, perhaps influencing cellular pathways.
  • Environmental Impact: Understanding compounds like this one is vital for assessing their ecological footprint, particularly in terms of biodegradability, persistence, and the impact on aquatic life.
  • Chemical Synthesis: The synthesis of such complex molecules often involves advanced techniques in organic chemistry, including multi-step synthesis and strategic functionalization. This aspect resonates strongly with chemistry students exploring synthetic routes.

The exploration of this compound not only exemplifies the beauty of organic synthesis but also underscores the importance of understanding intricate molecules within the context of modern science. As one advances in the study of such compounds, the potential for novel discoveries in medicinal and environmental chemistry becomes apparent.

Synonyms
(9S,10R,12R)-2,3,9,10,11,12-Hexahydro-10-methoxy-2,9-dimethyl-1-oxo-9,12-epoxy-1H-diindolo[1,2,3-fg:3',2',1'-kl]pyrrolo[3,4-i][1,6]benzodiazocine-10-carboxylic acid, methyl ester
Methyl 16-methoxy-4,15-dimethyl-3-oxo-28-oxa-4,14,19-triazaoctacyclo[12.11.2.115,18.02,6.07,27.08,13.019,26.020,25]octacosa-1,6,8,10,12,20,22,24,26-nonaene-16-carboxylate
KT-5823?