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9-Hydroperoxy-9-methylfluorene

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Identification
Molecular formula
C14H12O2
CAS number
26964-98-3
IUPAC name
9-hydroperoxy-9-methyl-fluorene
State
State

At room temperature, 9-Hydroperoxy-9-methylfluorene is generally found in the solid state. The solid form is due to the aggregated packing of its aromatic rings in the crystal lattice.

Melting point (Celsius)
143.00
Melting point (Kelvin)
416.15
Boiling point (Celsius)
329.30
Boiling point (Kelvin)
602.45
General information
Molecular weight
212.24g/mol
Molar mass
212.2410g/mol
Density
1.2740g/cm3
Appearence

9-Hydroperoxy-9-methylfluorene typically appears as a white to off-white crystalline solid. Its detailed crystallographic properties include structural characteristics pertinent to its aromatic fluorenyl moiety coupled with the hydroperoxy functional group.

Comment on solubility

Solubility of 9-hydroperoxy-9-methyl-fluorene

The solubility of 9-hydroperoxy-9-methyl-fluorene is an intriguing subject due to its unique structure, which can influence its behavior in various solvents. Understanding its solubility characteristics can be essential for applications in organic synthesis and material science. Here are some points to consider:

  • Polar vs. Non-polar Solvents: Due to the presence of the hydroperoxy group, it is likely that 9-hydroperoxy-9-methyl-fluorene exhibits varying solubility in polar and non-polar solvents.
  • Hydrogen Bonding: The hydroperoxy group may lead to potential hydrogen bonding interactions, enhancing solubility in polar solvents like water or alcohols.
  • Solvent Selection: Typical solvents to explore for solubility tests might include:
    • Water
    • Ethanol
    • Dimethyl sulfoxide (DMSO)
    • Benzene
  • Temperature Influence: Temperature can play a crucial role, as increased temperatures often enhance solubility for many organic compounds.

In conclusion, while the specific solubility data for 9-hydroperoxy-9-methyl-fluorene may not be extensively documented, predicting its solubility involves considering its polar and non-polar characteristics, potential for hydrogen bonding, and the choice of solvent. As with any compound, experimental determination remains the ultimate test for solubility behavior.

Interesting facts

Interesting Facts about 9-hydroperoxy-9-methyl-fluorene

The compound 9-hydroperoxy-9-methyl-fluorene is a fascinating example of an organic hydroperoxide. As a derivative of fluorene, it showcases unique characteristics and properties that make it noteworthy in chemical research. Here are some intriguing facts:

  • Formation of Hydroperoxides: The compound belongs to a class of chemicals known as hydroperoxides, which possess a distinctive –OOH functional group. This functionality is known for its reactivity, particularly in oxidation-reduction reactions.
  • Applications: 9-hydroperoxy-9-methyl-fluorene has potential applications in various fields, including materials science and organic synthesis. It can be utilized in the development of polymers and as an intermediate in the synthesis of more complex organic molecules.
  • Photochemistry: Hydroperoxides like this compound have been studied for their role in photochemical reactions. They can undergo decomposition under light, which can lead to the formation of radicals, making them of interest in the study of radical chemistry.
  • Safety Considerations: Due to the reactive nature of hydroperoxides, safety is paramount. These compounds can be hazardous and require careful handling to prevent decomposition and potential explosions.

As researchers delve deeper into the unique properties and reactions of compounds like 9-hydroperoxy-9-methyl-fluorene, they continue to uncover possibilities for innovation in chemical processes and material development. The study of this compound not only enhances our understanding of hydroperoxides but also contributes to broader applications in both academic and industrial chemistry.

Synonyms
9-Hydroperoxy-9-methylfluorene
18774-09-9
DTXSID30172082
9-MF-OOH
DTXCID5094573
CCRIS 4262
BRN 1964830
FLUOREN-9-YL HYDROPEROXIDE, 9-METHYL-
4-06-00-04869 (Beilstein Handbook Reference)
SCHEMBL28550784