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Benzoylpyridine

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Identification
Molecular formula
C12H9NO
CAS number
613-93-4
IUPAC name
phenyl(4-pyridyl)methanone
State
State

At room temperature, phenyl(4-pyridyl)methanone is in a solid state.

Melting point (Celsius)
102.00
Melting point (Kelvin)
375.15
Boiling point (Celsius)
326.00
Boiling point (Kelvin)
599.15
General information
Molecular weight
183.21g/mol
Molar mass
183.2090g/mol
Density
1.1450g/cm3
Appearence

Phenyl(4-pyridyl)methanone, also known as benzoylpyridine, is a white to light yellow crystalline powder. It is typically off-white when impure and has a slight aromatic odor.

Comment on solubility

Solubility of Phenyl(4-pyridyl)methanone

The solubility of phenyl(4-pyridyl)methanone (also known as 4-Pyridylphenyl ketone) can vary based on several factors, including the solvent used and the temperature. Here are some important points to consider:

  • Polar vs Non-Polar Solvents: This compound has both polar (the pyridine ring) and non-polar (the phenyl group) characteristics, which often results in good solubility in moderately polar solvents.
  • Solvent Examples: It is generally soluble in:
    • Dimethyl sulfoxide (DMSO)
    • Dimethylformamide (DMF)
    • Ethanol
  • Water Solubility: Typically, phenyl(4-pyridyl)methanone exhibits low solubility in water due to its organic structure.
  • Temperature Influence: As with many organic compounds, increasing the temperature may enhance its solubility in certain solvents.

In conclusion, understanding the solubility of phenyl(4-pyridyl)methanone is crucial for its application in various chemical reactions and processes. Its behavior in different solvents allows for practical usage in laboratories and industrial settings.

Interesting facts

Interesting Facts about Phenyl(4-pyridyl)methanone

Phemyl(4-pyridyl)methanone, an intriguing compound, boasts a variety of applications in both research and industry. Here are some captivating aspects of this compound:

  • Structural Significance: This compound features a unique structure, integrating a phenyl and a pyridyl group. The interplay between these aromatic systems lends the compound its intriguing chemical behavior.
  • Reactivity: As a ketone, it undergoes various reactions characteristic of carbonyl compounds, making it a versatile building block in organic synthesis.
  • Biological Relevance: Some derivatives of phenyl(4-pyridyl)methanone have been investigated for their potential biological activities, including antimicrobial and anti-inflammatory properties.
  • Material Science: Due to its aromatic nature, this compound can play roles in material science, particularly in the development of organic semiconductors and light-emitting diodes (LEDs).
  • Research Potential: The study of this compound not only broadens our understanding of ketones and their reactivity but also encourages exploration into novel reaction pathways and applications in complex molecule synthesis.

As emphasized by chemists, "The beauty of chemistry lies in its interconnectivity." Exploring compounds like phenyl(4-pyridyl)methanone exemplifies the vast possibilities that exist within the realm of organic chemistry.

Synonyms
4-Benzoylpyridine
14548-46-0
Phenyl 4-pyridyl ketone
Methanone, phenyl-4-pyridinyl-
Ketone, phenyl 4-pyridyl
Phenyl(4-pyridinyl)methanone
4-Pyridyl phenyl ketone
gamma-Benzoylpyridine
Ba 33215
524YQ3O21T
NSC-9488
DTXSID6022262
DTXCID202262
238-586-7
phenyl(pyridin-4-yl)methanone
Pyridine, 4-benzoyl-
4-benzoyl pyridine
.gamma.-Benzoylpyridine
NSC 9488
MFCD00006430
EINECS 238-586-7
BRN 0003864
UNII-524YQ3O21T
phenyl 4-pyridinyl ketone
ChemDiv2_000073
WLN: T6NJ DVR
phenyl(4-pyridyl)methanone
5-21-08-00576 (Beilstein Handbook Reference)
MLS000084817
SCHEMBL229650
SCHEMBL2888112
SCHEMBL8786624
CHEMBL1446524
SCHEMBL27395626
[(Pyridin-4-yl)carbonyl]benzene
NSC9488
CHEBI:194620
HMS1369D07
HMS2372M15
SBB032964
STK014114
AKOS000119486
CCG-103883
FB00812
SMR000019163
SY048792
DB-042783
B0306
CS-0109098
NS00053854
ST50406222
EN300-17901
H11247
AC-907/25014301
SR-01000399379
SR-01000399379-1
Q27260957
Z57069936
InChI=1/C12H9NO/c14-12(10-4-2-1-3-5-10)11-6-8-13-9-7-11/h1-9