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Quinone imine

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Identification
Molecular formula
C6H6O2
CAS number
2033-24-1
IUPAC name
N,N-dihydroxy-3,4-diimino-cyclohexa-1,5-dien-1-amine
State
State

At room temperature, Quinone imine is typically a solid. It is known for being relatively stable in its solid form, although it can be reactive or decompose under certain conditions.

Melting point (Celsius)
300.00
Melting point (Kelvin)
573.15
Boiling point (Celsius)
370.00
Boiling point (Kelvin)
643.15
General information
Molecular weight
110.10g/mol
Molar mass
110.0990g/mol
Density
1.6400g/cm3
Appearence

The compound typically appears as a crystalline solid that may have various shades ranging from yellow to brown depending on its purity.

Comment on solubility

Solubility of N,N-dihydroxy-3,4-diimino-cyclohexa-1,5-dien-1-amine

The solubility of N,N-dihydroxy-3,4-diimino-cyclohexa-1,5-dien-1-amine is influenced by its unique chemical structure and functional groups. This compound features multiple hydroxyl (-OH) and amino (-NH2) groups, which typically enhance solubility in polar solvents. However, several factors contribute to its actual solubility characteristics:

  • Polar Interactions: The presence of hydroxyl groups suggests that this compound may be soluble in water due to hydrogen bonding.
  • Hydrophobic Regions: Parts of the molecular structure may introduce hydrophobic characteristics, potentially limiting solubility in non-polar solvents.
  • Temperature Effects: Solubility tends to increase with temperature; thus, heating may aid in achieving higher solubility.
  • pH Dependence: The ionization of amino groups can vary with pH, impacting solubility in aqueous solutions.

In conclusion, while N,N-dihydroxy-3,4-diimino-cyclohexa-1,5-dien-1-amine may exhibit significant solubility in polar solvents due to its functional groups, its actual solubility must be determined through experimental conditions to account for the balance between its polar and non-polar characteristics.

Interesting facts

Interesting Facts about N,N-Dihydroxy-3,4-diimino-cyclohexa-1,5-dien-1-amine

N,N-dihydroxy-3,4-diimino-cyclohexa-1,5-dien-1-amine is a fascinating compound known for its unique molecular structure and intriguing chemical behavior. Here are some key points that science enthusiasts and chemistry students might find particularly interesting:

  • Structural Composition: This compound features a cyclohexadiene core that is characterized by its double bonds, which contribute to its reactivity and stability properties.
  • Functional Groups: The presence of the dihydroxy groups enhances its potential for hydrogen bonding, leading to various interactions with other molecules, making it a versatile compound in organic synthesis.
  • Applications in Research: Due to its unique properties, N,N-dihydroxy-3,4-diimino-cyclohexa-1,5-dien-1-amine is studied for potential applications in fields such as materials science, pharmaceuticals, and dye synthesis.
  • Reactivity: The imino groups in its structure suggest that it may participate in various chemical reactions, including nucleophilic additions and condensations, providing exciting pathways for chemical transformations.
  • Chemical Behavior: Scientists are particularly interested in the compound's redox properties, offering insights into electron transfer processes that are foundational in organic and bio-organic chemistry.

As a scientist or student studying this compound, you might find it especially intriguing to explore how slight modifications in its structure can lead to significantly different chemical properties and reactivity patterns. The world of complex organic compounds like N,N-dihydroxy-3,4-diimino-cyclohexa-1,5-dien-1-amine continues to inspire innovation in chemical research and applications!