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N-(9H-fluoren-2-yl)-N-hydroxy-benzamide

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Identification
Molecular formula
C20H15NO2
CAS number
61272-77-3
IUPAC name
N-(9H-fluoren-2-yl)-N-hydroxy-benzamide
State
State

At room temperature, N-(9H-fluoren-2-yl)-N-hydroxy-benzamide is typically in a solid state.

Melting point (Celsius)
228.00
Melting point (Kelvin)
501.15
Boiling point (Celsius)
395.20
Boiling point (Kelvin)
668.35
General information
Molecular weight
299.34g/mol
Molar mass
299.3200g/mol
Density
1.3124g/cm3
Appearence

N-(9H-fluoren-2-yl)-N-hydroxy-benzamide is typically found as a crystalline solid. It often appears as white to off-white crystals, indicating its purity and purity-related properties.

Comment on solubility

Solubility of N-(9H-fluoren-2-yl)-N-hydroxy-benzamide

N-(9H-fluoren-2-yl)-N-hydroxy-benzamide is a compound showing unique solubility characteristics. Upon examination, we can highlight the following aspects:

  • Apolar Nature: The compound's structure contains bulky fluorene moieties that influence its overall polarity and solubility behavior in various solvents.
  • Solvent Compatibility: Typically, this compound is more soluble in nonpolar organic solvents such as toluene and chloroform, while showing significantly lower solubility in water.
  • Hydroxy Group Impact: The presence of the –OH (hydroxy) group may provide some hydrogen bonding capability, potentially enhancing solubility in polar solvents, but the overall bulky structure can impede this.

It is important to note that the solubility behavior can be influenced by:

  1. The concentration of the compound.
  2. Temperature variations, which can lead to increased solubility in certain solvents.
  3. The presence of other solutes or impurities that may affect the solvation process.

In conclusion, while N-(9H-fluoren-2-yl)-N-hydroxy-benzamide exhibits some solubility in select organic solvents, its significant structural attributes largely dictate its behavior, rendering it less soluble in aqueous environments.

Interesting facts

Interesting Facts About N-(9H-fluoren-2-yl)-N-hydroxy-benzamide

N-(9H-fluoren-2-yl)-N-hydroxy-benzamide, often referred to in research contexts, is a fascinating compound that has garnered attention in organic chemistry and medicinal research. Here are some intriguing points to consider:

  • Dual Functionality: This compound possesses both a hydroxyl group and a benzamide function, which significantly enhance its reactivity and potential applications in synthesis and biological activity.
  • Fluorene moiety: The presence of the 9H-fluoren structure contributes to its unique properties, offering a planar, rigid framework that is often encountered in organic electronics and photonic devices.
  • Biological Applications: Research indicates that compounds similar to N-(9H-fluoren-2-yl)-N-hydroxy-benzamide have potential as inhibitors in various biochemical pathways, presenting opportunities for drug development against diseases.
  • Ligand Properties: The compound can act as a ligand in coordination chemistry, influencing the behavior of metal ions in different reactions, thus expanding its utility in catalysis.
  • Research Interest: Ongoing studies focus on this compound due to its structural features, which may allow for the development of new materials with desirable electronic or optical properties.

In conclusion, N-(9H-fluoren-2-yl)-N-hydroxy-benzamide serves as a remarkable compound with diverse implications in both synthetic chemistry and potential therapeutic avenues. Its unique structure invites chemists to explore innovative applications in various fields.

Synonyms
N-Hydroxy-N-(2-fluorenyl)benzamide
N-Hydroxy-N-2-fluorenylbenzamide
CCRIS 2719
N-Hydroxy-2-benzoylaminofluorene
N-Benzoyloxy-acetylaminofluorene
QS2A8UW3HC
N-Fluoren-2-ylbenzohydroxamic acid
BRN 2758983
DTXSID20190174
N-9H-FLUOREN-2-YL-N-HYDROXYBENZAMIDE
N-OH-2-FBA
DTXCID30112665
3671-71-4
N-(9H-fluoren-2-yl)-N-hydroxybenzamide
Benzamide, N-9H-fluoren-2-yl-N-hydroxy-
BENZOHYDROXAMIC ACID, N-FLUOREN-2-YL-
UNII-QS2A8UW3HC
CHEMBL311673