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N-(4-hydroxy-5-oxo-cyclohepta-1,3,6-trien-1-yl)benzamide

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Identification
Molecular formula
C14H9NO3
CAS number
132123-09-0
IUPAC name
N-(4-hydroxy-5-oxo-cyclohepta-1,3,6-trien-1-yl)benzamide
State
State
The compound is in a solid state at room temperature, and it is typically stable under standard laboratory conditions.
Melting point (Celsius)
201.50
Melting point (Kelvin)
474.65
Boiling point (Celsius)
498.00
Boiling point (Kelvin)
771.15
General information
Molecular weight
237.07g/mol
Molar mass
237.0740g/mol
Density
1.3078g/cm3
Appearence

The compound appears as a crystalline solid with a pale yellow color, which may vary slightly depending on the purity and synthesis method used.

Comment on solubility

Solubility of N-(4-hydroxy-5-oxo-cyclohepta-1,3,6-trien-1-yl)benzamide

The solubility of N-(4-hydroxy-5-oxo-cyclohepta-1,3,6-trien-1-yl)benzamide is a multifaceted subject, influenced by its unique structural characteristics. Understanding the solubility behavior of this compound is essential for various applications in chemical and pharmaceutical fields.

Factors Affecting Solubility

Several factors contribute to the solubility profile of this compound:

  • Polarity: The presence of hydroxyl groups can increase solubility in polar solvents.
  • Hydrogen Bonding: The ability to form hydrogen bonds enhances interactions with solvents.
  • Molecular Weight: Generally, lower molecular weight compounds tend to be more soluble.

Solvent Compatibility

N-(4-hydroxy-5-oxo-cyclohepta-1,3,6-trien-1-yl)benzamide exhibits varying degrees of solubility in:

  • Aqueous Solutions: Limited solubility is expected due to its organic structure.
  • Organic Solvents: Better solubility in solvents like ethanol or DMSO may occur, owing to similar polar characteristics.

In summary, the solubility of N-(4-hydroxy-5-oxo-cyclohepta-1,3,6-trien-1-yl)benzamide can be described as moderate, emphasizing the importance of solvent selection for effective utilization. As the wise saying goes, "Like dissolves like," underscoring the need for careful consideration of solvents when working with this intriguing compound.

Interesting facts

Interesting Facts about N-(4-hydroxy-5-oxo-cyclohepta-1,3,6-trien-1-yl)benzamide

N-(4-hydroxy-5-oxo-cyclohepta-1,3,6-trien-1-yl)benzamide is a fascinating compound that showcases the intricate relationship between organic chemistry and medicinal applications. This compound possesses unique structural features that make it a subject of interest among researchers and students alike. Here are some intriguing aspects:

  • Cyclic Structure: The presence of a cycloheptatriene core in its structure provides this compound with interesting reactivity and stability properties, often contributing to its biological activity.
  • Medicinal Potential: Compounds like benzamides have been studied for their pharmacological properties, including anti-inflammatory and analgesic effects. This highlights the potential for N-(4-hydroxy-5-oxo-cyclohepta-1,3,6-trien-1-yl)benzamide in drug development.
  • Hydroxyl Group Influence: The presence of the hydroxyl group (–OH) plays a crucial role in enhancing the compound's solubility and reactivity, making it interesting for synthesizing derivatives with improved properties.
  • Research Implications: Exploratory studies focus on how this compound interacts within biological systems, particularly its role in enzyme inhibition and other metabolic pathways, which could lead to therapeutic discoveries.
  • Structural Versatility: The molecular design permits possible modifications to create new analogs, which can have varied activities—a rich field for synthetic chemists.

Understanding N-(4-hydroxy-5-oxo-cyclohepta-1,3,6-trien-1-yl)benzamide goes beyond just its chemical composition; it connects to larger themes in chemistry, including the quest for effective therapeutics and the interplay of molecular structures with biological functions. As noted by some researchers, "The architecture of this compound not only reveals the elegance of chemical synthesis but also the vast potential for future innovations."

In summary, the study of this compound offers valuable insights into both fundamental chemistry and applied sciences, making it an exciting area for ongoing research.

Synonyms
19281-37-9
5-Benzamido-2-hydroxy-2,4,6-cycloheptatrien-1-one
0LFV92J0J8
2,4,6-CYCLOHEPTATRIEN-1-ONE, 5-BENZAMIDO-2-HYDROXY-
Benzamide, N-(4-hydroxy-5-oxo-1,3,6-cycloheptatrien-1-yl)-
NSC-79556
NSC 79556
BRN 2941410
NSC79556
Benzamide, N-(2-hydroxy-1-oxo-2,4,6-cycloheptatrienyl)-
WLN: L7VJ BQ EMVR
NCIOpen2_004648
UNII-0LFV92J0J8
SCHEMBL16749032
DTXSID60172878
Benzamide,4,6-cycloheptatrienyl)-
Benzamide,3,6-cycloheptatrien-1-yl)-
5-Benzamido-2-hydroxy-2,6-cycloheptatrien-1-one
2,6-Cycloheptatrien-1-one, 5-benzamido-2-hydroxy-
N-(4-HYDROXY-5-OXO-1,3,6-CYCLOHEPTATRIEN-1-YL)BENZAMIDE