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N-(4-carbamimidoylphenyl)-2-hydroxy-benzamide

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Identification
Molecular formula
C14H13N3O2
CAS number
34839-13-9
IUPAC name
N-(4-carbamimidoylphenyl)-2-hydroxy-benzamide
State
State

At room temperature, N-(4-carbamimidoylphenyl)-2-hydroxy-benzamide is in a solid state. It maintains its structure under normal laboratory conditions.

Melting point (Celsius)
285.00
Melting point (Kelvin)
558.20
Boiling point (Celsius)
492.50
Boiling point (Kelvin)
765.70
General information
Molecular weight
255.27g/mol
Molar mass
255.2670g/mol
Density
1.4532g/cm3
Appearence

N-(4-carbamimidoylphenyl)-2-hydroxy-benzamide typically appears as a crystalline solid. It is usually white or off-white in color.

Comment on solubility

Solubility of N-(4-carbamimidoylphenyl)-2-hydroxy-benzamide

N-(4-carbamimidoylphenyl)-2-hydroxy-benzamide, with the chemical formula C14H13N3O2, exhibits particular solubility characteristics that can be attributed to its molecular structure. Understanding its solubility is crucial for various applications in the field of chemistry, particularly in pharmaceuticals and organic synthesis.

Solubility Characteristics

This compound can be analyzed based on the following points:

  • Polarity: The presence of both hydroxyl (–OH) and amide (–NH–) functional groups suggests a degree of polarity, which may enhance its solubility in polar solvents such as water or methanol.
  • Hydrogen Bonding: The ability to form hydrogen bonds due to the –OH and amide groups contributes to solubility in aqueous environments.
  • Solvent Compatibility: It is likely to show better solubility in organic solvents compared to non-polar solvents due to its polar functional groups.
  • Concentration and Temperature Influence: As with many compounds, solubility may increase with temperature and concentration, providing practical considerations for experimental applications.

In summary, while the precise solubility values may vary based on specific conditions, the functional groups present in N-(4-carbamimidoylphenyl)-2-hydroxy-benzamide suggest that it is generally soluble in polar solvents. This solubility profile is essential for its utilization in various chemical contexts.

Interesting facts

Interesting Facts About N-(4-carbamimidoylphenyl)-2-hydroxy-benzamide

N-(4-carbamimidoylphenyl)-2-hydroxy-benzamide is a fascinating compound with unique properties and applications in various fields of science. Here are some key insights:

  • Structural Significance: The compound features a complex structure that includes both carbamimidoyl and hydroxy functional groups, which play a pivotal role in its reactivity and biological activity.
  • Potential Pharmaceutical Applications: Due to its unique molecular arrangement, this compound is of interest in medicinal chemistry for its potential therapeutic effects, particularly in the treatment of diseases linked to imbalances in specific biochemical pathways.
  • Research and Development: Ongoing research may explore its use as an inhibitor or modulator of certain enzymes, which could lead to the development of novel drug candidates.
  • Mechanistic Studies: Scientists are intrigued by the mechanism of action of this compound at a molecular level, including how it interacts with various biological targets.
  • Analytical Techniques: The characterization of N-(4-carbamimidoylphenyl)-2-hydroxy-benzamide often employs advanced analytical techniques such as NMR spectroscopy and mass spectrometry, shedding light on its structure and purity.

In summary, N-(4-carbamimidoylphenyl)-2-hydroxy-benzamide represents a rich area of research in chemistry and pharmacology. Its unique properties and potential applications make it a compound worth studying. Researchers continue to explore its capabilities, pushing the boundaries of our understanding in the chemical sciences.

Synonyms
n-(4-carbamimidoyl-phenyl)-2-hydroxy-benzamide
CHEMBL64708
N-(4-carbamimidoylphenyl)-2-hydroxybenzamide
1gja
SCHEMBL7244941
BDBM14155
MYHDBRFFPZXDMX-UHFFFAOYSA-N
APC-7136
Q27451646