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Octahydro-3H-naphtho[2,1-f]chromene-2,8-dione

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Identification
Molecular formula
C16H20O3
CAS number
486-30-8
IUPAC name
10a,12a-dimethyl-4,4a,4b,5,6,10b,11,12-octahydro-3H-naphtho[2,1-f]chromene-2,8-dione
State
State
Solid at room temperature, usually forming white to light yellow crystals or powder.
Melting point (Celsius)
196.00
Melting point (Kelvin)
469.15
Boiling point (Celsius)
505.00
Boiling point (Kelvin)
778.15
General information
Molecular weight
262.33g/mol
Molar mass
262.3340g/mol
Density
1.3200g/cm3
Appearence

The compound typically appears as a solid, with the possibility of being in crystalline or amorphous form depending on the exact conditions and method of synthesis.

Comment on solubility

Solubility of 10a,12a-dimethyl-4,4a,4b,5,6,10b,11,12-octahydro-3H-naphtho[2,1-f]chromene-2,8-dione

The compound 10a,12a-dimethyl-4,4a,4b,5,6,10b,11,12-octahydro-3H-naphtho[2,1-f]chromene-2,8-dione (C16H20O3) exhibits interesting solubility properties that are essential for its practical applications. Understanding its solubility behavior can help predict its behavior in various environments.

Solubility Characteristics

  • Solvent Dependency: The solubility of this compound is highly dependent on the nature of the solvent used. Non-polar solvents may enhance its solubility due to its predominantly hydrophobic structure.
  • Temperature Influence: Typically, increasing temperature can improve the solubility of organic compounds, including this one, allowing for the dissolution of more solid material into liquid.
  • Polarity Effects: Given the presence of functional groups, the solubility may increase in polar solvents like ethanol or dimethyl sulfoxide (DMSO), but it is less soluble in water due to its non-polar characteristics.

To summarize, the solubility of C16H20O3 can be considered:

  • Higher in organic solvents
  • Possibly increased by elevated temperatures
  • Limited in aqueous environments

In conclusion, understanding the solubility of this compound enhances not only its usability in chemical reactions but also its application across various industries. Exploring these parameters offers valuable insights into its behavior in different chemical contexts.

Interesting facts

Interesting Facts about 10a,12a-Dimethyl-4,4a,4b,5,6,10b,11,12-octahydro-3H-naphtho[2,1-f]chromene-2,8-dione

This compound is a fascinating example of a complex organic molecule that showcases the creativity found in chemical structures. With its unique arrangement, it plays a significant role in a variety of scientific fields. Here are some engaging facts that illustrate its importance:

  • Structural Complexity: The intricate structure of this compound includes a naphtho[2,1-f]chromene framework, which is essential for many natural products and pharmacologically active substances.
  • Natural Product Inspiration: Compounds similar to this structure are often found in many plants and contribute to their therapeutic properties. This connects chemistry with botany and medicine.
  • Potential Applications: Researchers explore the synthesis of this compound for its potential use in drug development, particularly in targeting diseases such as cancer due to similar compounds' bioactivity.
  • Unique Functional Groups: The presence of both dione and alkyl modifications implies specific chemical reactivity that could lead to innovative applications in material sciences.
  • Electronics and Materials: The unique electronic properties of compounds with such complex cyclic structures make them potential candidates for organic electronics, such as OLEDs (Organic Light Emitting Diodes).

Moreover, the investigation of 10a,12a-dimethyl-4,4a,4b,5,6,10b,11,12-octahydro-3H-naphtho[2,1-f]chromene-2,8-dione is an excellent illustration of how the study of organic compounds goes beyond academia into real-world applications. As scientists delve deeper into its properties, they uncover new implications that could shape future innovations.

As the renowned chemist Linus Pauling once said, "The best way to have a good idea is to have a lot of ideas." This holds true in the exploration of complex chemical compounds, where the potential for discovery is endless.

Synonyms
Teslak
.DELTA.1-Testololactone
.DELTA.1-Dehydrotestolactone
.DELTA.1-Dehydrotestololactone
NSC 12173
CHEMBL166839
DTXSID10859561
BPEWUONYVDABNZ-UHFFFAOYSA-N
17a-Oxa-D-homoandrosta-1,4-diene-3,17-dione
13,17-Secoandrosta-1,4-dien-17-oic acid, 13-hydroxy-3-oxo-, .delta.-lactone
13-Hydroxy-3-oxo-13,17-secoandrosta-1,4-dien-17-oic acid .delta.-lactone
10a,12a-Dimethyl-3,4,4a,5,6,10a,10b,11,12,12a-decahydro-2H-naphtho[2,1-f]chromene-2,8(4bH)-dione #
10a,12a-Dimethyl-3,4,4a,5,6,10a,10b,11,12,12a-decahydro-2H-phenanthro[2,1-b]pyran-2,8(4bH)-dione
2H-Phenanthro(2,1-b)pyran-2,8(4bH)-dione, 3,4,4a,5,6,10a,10b,11,12,12a-decahydro-10a,12a-dimethyl-, , [4aS-(4a.alpha.,4b.beta.,10a.beta.,10b.alpha.,12a.beta.)]-