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3-(dihydroxyamino)-5-(2-fluorobenzoyl)-1,2-benzoquinone

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Identification
Molecular formula
C14H8FNO4
CAS number
1786-33-0
IUPAC name
3-(dihydroxyamino)-5-(2-fluorobenzoyl)-1,2-benzoquinone
State
State

At room temperature, this compound exists as a solid, maintaining its structure unless subjected to temperatures close to its melting point. Proper storage involves keeping it in a cool, dry place to prevent degradation or unwanted reaction.

Melting point (Celsius)
178.00
Melting point (Kelvin)
451.15
Boiling point (Celsius)
375.00
Boiling point (Kelvin)
648.15
General information
Molecular weight
275.23g/mol
Molar mass
275.2310g/mol
Density
1.4800g/cm3
Appearence

The compound is typically found as a crystalline solid with a light yellow to pale orange color. It may exhibit a distinct crystalline structure when observed under a microscope. The appearance can vary with purity and preparation methods, making it important to handle the compound with care to maintain its integrity.

Comment on solubility

Solubility of 3-(dihydroxyamino)-5-(2-fluorobenzoyl)-1,2-benzoquinone (C14H8FNO4)

The solubility of 3-(dihydroxyamino)-5-(2-fluorobenzoyl)-1,2-benzoquinone is influenced by several factors, making it a compound of interest in various fields.

  • Polarity: Given the presence of both hydroxyl (-OH) groups and a fluorine substituent, the compound exhibits a mixture of polar and non-polar characteristics.
  • Solvent Interaction: This duality suggests that the compound may have enhanced solubility in polar solvents like water, as well as in organic solvents due to its aromatic structure.
  • Temperature Dependence: Solubility may increase with temperature, which is a common characteristic for many organic compounds.
  • pH Sensitivity: The presence of hydroxylamine moieties can lead to changes in solubility under varying pH conditions, potentially making it more soluble in acidic or basic environments.

Overall, while the specific solubility data for 3-(dihydroxyamino)-5-(2-fluorobenzoyl)-1,2-benzoquinone may not be readily available, we can anticipate a favorable solubility profile based on its chemical structure. This characteristic could have significant implications for its applications in pharmaceuticals and materials science.

Interesting facts

Interesting Facts about 3-(Dihydroxyamino)-5-(2-fluorobenzoyl)-1,2-benzoquinone

This fascinating compound falls under the category of benzoquinones, which are known for their unique reactivity and contributions to various biological systems. Here are some noteworthy points:

  • Biological Significance: Compounds like 3-(dihydroxyamino)-5-(2-fluorobenzoyl)-1,2-benzoquinone play vital roles in biological pathways, particularly in redox reactions, due to their ability to undergo electron transfer. This feature makes them potential candidates in the development of pharmaceuticals.
  • Fluorine Influence: The incorporation of a fluorobenzoyl group can significantly affect the compound's chemical behavior and biological activity. Fluorine substitution is often linked to enhanced metabolic stability and lipophilicity, which can optimize bioavailability.
  • Antioxidant Properties: Benzoquinones, including this compound, have been studied for their antioxidant capabilities. Their structure allows for the modulation of reactive oxygen species (ROS), contributing to cellular signaling and protective mechanisms within organisms.
  • Potential Applications: Due to its unique structure, this compound could have potential applications in materials science and organic electronics, particularly in the design of organic semiconductors or sensors.
  • Research Opportunities: The intricate nature of 3-(dihydroxyamino)-5-(2-fluorobenzoyl)-1,2-benzoquinone presents numerous avenues for research. Scientists are continually exploring its synthesis, reactivity patterns, and interactions within biological systems.

In the words of chemist Linus Pauling, “The secret of life is in the chemistry,” and compounds like this exemplify the intricate relationship between chemical structure and function, offering endless possibilities for discovery.