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2,4,6-Cycloheptatrien-1-one, 5-amino-2-hydroxy-

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Identification
Molecular formula
C7H7NO2
CAS number
Not available
IUPAC name
5-amino-2-hydroxy-cyclohepta-2,4,6-trien-1-one
State
State

At room temperature, the compound is a solid, displaying a distinct appearance which makes it easy to identify during handling and use within various applications in the laboratory.

Melting point (Celsius)
170.00
Melting point (Kelvin)
443.00
Boiling point (Celsius)
340.00
Boiling point (Kelvin)
613.00
General information
Molecular weight
137.15g/mol
Molar mass
137.1510g/mol
Density
1.3500g/cm3
Appearence

The compound appears as a yellow crystalline solid. It exhibits a characteristic light yellow color due to the conjugated system present in the cyclic structure.

Comment on solubility

Solubility of 5-amino-2-hydroxy-cyclohepta-2,4,6-trien-1-one

The solubility of 5-amino-2-hydroxy-cyclohepta-2,4,6-trien-1-one reflects the compound's unique structural characteristics. Factors influencing its solubility include:

  • Polarity: The presence of both amino (-NH2) and hydroxy (-OH) groups indicates potential hydrogen bonding, which often enhances solubility in polar solvents such as water.
  • Hydrophobic Regions: The cyclic structure and the nature of the double bonds within the compound may introduce hydrophobic characteristics, which can limit solubility in polar environments.
  • Solvent Interaction: This compound may exhibit variable solubility depending on the solvent used — its solubility could be greater in organic solvents than in water due to its cycloheptatriene framework.

It is essential to consider that the degree of ionization of the functional groups in various pH environments can also impact solubility:

  • In acidic conditions, the amino group may protonate, enhancing solubility in the aqueous phase.
  • In basic conditions, the hydroxyl group may become deprotonated, further affecting solubility dynamics.

Overall, the solubility of 5-amino-2-hydroxy-cyclohepta-2,4,6-trien-1-one is complex and likely varies significantly with changes in environmental conditions and the choice of solvent. As with many organic compounds, experimental determination is vital for precise solubility assessments.

Interesting facts

Introducing 5-amino-2-hydroxy-cyclohepta-2,4,6-trien-1-one

5-amino-2-hydroxy-cyclohepta-2,4,6-trien-1-one is a fascinating compound that exhibits various intriguing characteristics. This compound belongs to the family of amino phenols and aromatic ketones, making it a subject of interest both in organic chemistry and medicinal applications. Here are some notable facts about this compound:

Key Features

  • Amino Group: The presence of an amino group (-NH2) makes this compound a potential candidate for various chemical reactions, including nucleophilic substitutions and condensation reactions.
  • Hydroxy Group: The hydroxy group (-OH) contributes to the compound's reactivity, enabling hydrogen bonding which can enhance its solubility in polar solvents.
  • Cyclic Structure: The cycloheptatriene structure brings about unique resonance stabilization, which can influence the reactivity and stability of the compound.

Potential Applications

This compound is not just an academic curiosity but holds promise in several fields:

  • Pharmaceuticals: Compounds with similar structures have been studied for their bioactive properties, including antitumor and antimicrobial activities.
  • Dyes and Pigments: Thanks to the conjugated system present in its structure, it may be explored for applications in dye synthesis.
  • Material Science: Its unique properties may lend themselves to research in developing new materials or catalysts.

Conclusion

In summary, 5-amino-2-hydroxy-cyclohepta-2,4,6-trien-1-one stands as a compound of great interest due to its structural uniqueness and potential applications in various scientific fields. As research continues to unveil the properties and reactions of such compounds, further insights into their uses could emerge, demonstrating the importance of understanding even the most complex chemical structures.

Synonyms
5-Aminotropolone
7021-46-7
5-amino-2-hydroxycyclohepta-2,4,6-trien-1-one
VII tropolone
2,4,6-CYCLOHEPTATRIEN-1-ONE, 5-AMINO-2-HYDROXY-
5-Amino-2-hydroxy-2,4,6-cycloheptatrien-1-one
2-Hydroxy-5-amino-2,4,6-cycloheptatriene-1-one
NSC-102877
NSC 102877
BRN 1524779
NSC102877
tropolone, 5-amino-
FM98CTZ6ZR
SCHEMBL916337
DTXSID90990446
HAA02146
AKOS006340973
EN300-658853
5-amino-2-hydroxy-2,4,6 -cycloheptatrien-1-one
5-amino-2-hydroxy-2,4,6-cycloheptatriene-1-one
F9994-0566
Z1203578162