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Camptothecin

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Identification
Molecular formula
C20H16N2O4
CAS number
7689-03-4
IUPAC name
methyl 11-acetoxy-12-ethyl-10-hydroxy-8-methyl-8,16-diazapentacyclo[10.6.1.01,9.02,7.016,19]nonadeca-2,4,6,13-tetraene-3-carboxylate
State
State

At room temperature, Camptothecin is a solid compound.

Melting point (Celsius)
264.00
Melting point (Kelvin)
537.00
Boiling point (Celsius)
583.00
Boiling point (Kelvin)
856.00
General information
Molecular weight
348.35g/mol
Molar mass
348.3530g/mol
Density
1.4304g/cm3
Appearence

Camptothecin is a pale yellow crystalline powder. It is sensitive to light and tends to degrade when exposed to it.

Comment on solubility

Solubility of Methyl 11-acetoxy-12-ethyl-10-hydroxy-8-methyl-8,16-diazapentacyclo[10.6.1.01,9.02,7.016,19]nonadeca-2,4,6,13-tetraene-3-carboxylate

The solubility of methyl 11-acetoxy-12-ethyl-10-hydroxy-8-methyl-8,16-diazapentacyclo[10.6.1.01,9.02,7.016,19]nonadeca-2,4,6,13-tetraene-3-carboxylate is an intriguing aspect of its chemical behavior. Factors influencing its solubility include:

  • Molecular Structure: The presence of functional groups such as acetoxy and hydroxy can increase the compound's polarity.
  • Polarity: Generally, polar compounds are more soluble in polar solvents, while non-polar compounds dissolve better in non-polar solvents.
  • Hydrogen Bonding: The hydroxy group may form hydrogen bonds with water, potentially enhancing solubility in aqueous environments.
  • Chain Length: The length and branching of the hydrocarbon chains in the structure can influence how well it interacts with solvents.

For practical consideration, its solubility can be described as:

  1. High: Expect greater solubility in polar solvents like water.
  2. Moderate: May exhibit variable solubility in organic solvents depending on the specific solvent's characteristics.
  3. Low: Limited solubility in highly non-polar solvents.

In summary, while specific solubility data may be scarce, it can be anticipated that methyl 11-acetoxy-12-ethyl-10-hydroxy-8-methyl-8,16-diazapentacyclo[10.6.1.01,9.02,7.016,19]nonadeca-2,4,6,13-tetraene-3-carboxylate will exhibit varied solubility behaviors influenced by its complex structure and the solvents used.

Interesting facts

Interesting Facts about Methyl 11-acetoxy-12-ethyl-10-hydroxy-8-methyl-8,16-diazapentacyclo[10.6.1.01,9.02,7.016,19]nonadeca-2,4,6,13-tetraene-3-carboxylate

Methyl 11-acetoxy-12-ethyl-10-hydroxy-8-methyl-8,16-diazapentacyclo[10.6.1.01,9.02,7.016,19]nonadeca-2,4,6,13-tetraene-3-carboxylate is a complex organic compound that belongs to a class of molecules known for their intricate structures and functional groups. Here are some fascinating insights into this compound:

  • Structural Complexity: The unique pentacyclic structure showcases the compound's intricate connectivity, which can present challenges and opportunities in synthetic chemistry.
  • Biological Significance: Compounds with similar frameworks have been investigated for their potential biological activities, including anti-cancer and anti-inflammatory properties, making them of interest in pharmacological research.
  • Functional Groups: The presence of multiple functional groups, such as acetoxy and hydroxy, contributes to the reactivity and possible applications in organic synthesis.
  • Potential Applications: This compound could serve as a precursor for developing new materials, particularly in the fields of drug design and nanotechnology.

As you delve into the world of organic chemistry, consider the significance of such compounds where the complexity of their structure can lead to unique properties and multidisciplinary applications. Indeed, it is within these intricate designs that scientists often find inspiration for novel solutions in various fields.

"In chemistry, complexity often begets beauty and functionality." This notion rings especially true when studying compounds like methyl 11-acetoxy-12-ethyl-10-hydroxy-8-methyl-8,16-diazapentacyclo[10.6.1.01,9.02,7.016,19]nonadeca-2,4,6,13-tetraene-3-carboxylate, where the interplay of structure and reactivity can lead to groundbreaking discoveries.

Synonyms
AKOS032948116
methyl 11-(acetyloxy)-12-ethyl-10-hydroxy-8-methyl-8,16-diazapentacyclo[10.6.1.0(1),?.0(2),?.0(1)?,(1)?]nonadeca-2,4,6,13-tetraene-3-carboxylate