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11-methyl-3,4-dihydro-2H-chrysen-1-one

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Identification
Molecular formula
C18H16O
CAS number
7478-32-6
IUPAC name
11-methyl-3,4-dihydro-2H-chrysen-1-one
State
State
The compound is typically found in a solid state at room temperature and under standard conditions.
Melting point (Celsius)
132.00
Melting point (Kelvin)
405.15
Boiling point (Celsius)
424.50
Boiling point (Kelvin)
697.65
General information
Molecular weight
246.33g/mol
Molar mass
246.3280g/mol
Density
1.2225g/cm3
Appearence

The compound 11-methyl-3,4-dihydro-2H-chrysen-1-one typically appears as a crystalline solid. The exact color and form can vary, but it is usually white to pale yellow, reflecting its polycyclic aromatic structure.

Comment on solubility

Solubility of 11-methyl-3,4-dihydro-2H-chrysen-1-one

The solubility of 11-methyl-3,4-dihydro-2H-chrysen-1-one in various solvents can vary significantly due to its unique structural features. This compound is generally considered to be a non-polar hydrophobic molecule, which typically leads to low solubility in polar solvents like water.

Key points to consider regarding its solubility include:

  • Solvent Compatibility: It is likely to be more soluble in non-polar organic solvents such as hexane, toluene, or chloroform.
  • Temperature Dependence: Increasing the temperature may enhance solubility in organic solvents due to greater molecular motion.
  • Hydrophobic Effects: The compound’s hydrophobic characteristics can limit its interactions with polar solvents, thus decreasing solubility.

In summary, 11-methyl-3,4-dihydro-2H-chrysen-1-one exhibits a solubility profile that favors non-polar mediums while exhibiting minimal interaction with water-based solutions. Proper solvent selection is crucial for applications involving this compound.

Interesting facts

Interesting Facts about 11-Methyl-3,4-dihydro-2H-chrysen-1-one

11-Methyl-3,4-dihydro-2H-chrysen-1-one is a fascinating compound that has sparked interest in various fields of research, particularly in organic chemistry and medicinal applications. Here are some engaging facts about this unique molecule:

  • Structural Characteristics: This compound is part of the chrysenone family, characterized by its polycyclic structure, which exhibits unique properties due to the arrangement of its rings.
  • Synthetic Routes: The synthesis of 11-methyl-3,4-dihydro-2H-chrysen-1-one is often accomplished through multi-step chemical reactions, highlighting the importance of reaction conditions and catalysts in organic synthesis.
  • Biological Activity: Compounds such as this one have been studied for their potential therapeutic properties, making them of significant interest in pharmacology. Some derivatives are explored for their efficacy as anti-cancer agents.
  • Materials Science: Due to its unique electronic structure, this compound may also find applications in materials science, particularly in the development of organic semiconductor devices.
  • Research Potential: Researchers continue to explore the properties and reactions of 11-methyl-3,4-dihydro-2H-chrysen-1-one, offering a wealth of opportunities for discovering new compounds and materials.

As always, the journey of understanding compounds like 11-methyl-3,4-dihydro-2H-chrysen-1-one showcases the intricate beauty of chemistry, where each molecule can hold the key to scientific advancement. Embracing the complexity of such compounds invariably leads to ground-breaking innovations!

Synonyms
27343-29-9
Chrysene-11-methyl-1,2,3,4-tetrahydro-1-one
1(2H)-Chrysenone, 3,4-dihydro-11-methyl-
1,2,3,4-Tetrahydro-11-methylchrysen-1-one
CHRYSEN-1-ONE, 1,2,3,4-TETRAHYDRO-11-METHYL-
BRN 2467027
11-Methyl-3,4-dihydro-1(2H)-chrysenone
11-Methyl-1-oxo-1,2,3,4-tetrahydrochrysene
3,4-Dihydro-11-methyl-1(2H)-Chrysenone
3-07-00-02658 (Beilstein Handbook Reference)
P6S49KR37L
DTXSID10181778