Skip to main content

Benzoylformaldehyde

ADVERTISEMENT
Identification
Molecular formula
C8H6O2
CAS number
4461-30-7
IUPAC name
2-oxo-2-phenyl-acetaldehyde
State
State
At room temperature, Benzoylformaldehyde can be found either as a yellow liquid or as a light solid, depending on the ambient conditions.
Melting point (Celsius)
41.00
Melting point (Kelvin)
314.00
Boiling point (Celsius)
232.00
Boiling point (Kelvin)
505.00
General information
Molecular weight
134.13g/mol
Molar mass
134.1310g/mol
Density
1.1660g/cm3
Appearence

Benzoylformaldehyde appears as a pale yellow liquid or light solid with a distinct aromatic odor. It can exist in different forms depending on temperature.

Comment on solubility

Solubility of 2-oxo-2-phenyl-acetaldehyde

When discussing the solubility of 2-oxo-2-phenyl-acetaldehyde (C9H8O2), we should consider several key factors:

  • Polarity: Due to the presence of both an aldehyde group and a ketone group, this compound exhibits a degree of polarity, which influences its solubility in various solvents.
  • Solvent Compatibility: 2-oxo-2-phenyl-acetaldehyde is generally soluble in polar solvents such as alcohols and ethers. However, it may have limited solubility in non-polar solvents.
  • Temperature Effects: Like many organic compounds, its solubility can increase with temperature, enabling it to dissolve better in higher-temperature solvents.
  • Hydrogen Bonding: This compound has the potential to engage in hydrogen bonding with solvents that have -OH or -NH groups, further enhancing its solubility profile.

In summary, 2-oxo-2-phenyl-acetaldehyde demonstrates appreciable solubility in polar solvents due to its polar functional groups, making it versatile for various applications in chemical reactions. Remember, the solubility characteristics can be critical for predicting how this compound behaves in different environments.

Interesting facts

Interesting Facts about 2-Oxo-2-phenylacetaldehyde

2-Oxo-2-phenylacetaldehyde, a compound with a captivating chemical structure, is known for its distinct properties and versatile applications. Here are some fascinating insights:

  • Functional Groups: This compound features both an aldehyde and a ketone functional group, making it interesting for various organic synthesis reactions.
  • Synthetic Applications: 2-Oxo-2-phenylacetaldehyde is utilized as an intermediate in the synthesis of pharmaceutical compounds. Its reactivity can facilitate the creation of more complex structures, particularly in drug discovery.
  • Flavor and Fragrance: It possesses aromatic characteristics, allowing it to be explored in the fragrance industry. Compounds like this often contribute to the scent profiles of certain perfumes and flavorings.
  • Chemical Reactions: The compound is prone to participate in various chemical reactions, such as condensation and Michael addition, showcasing its versatility in organic chemistry.
  • Biological Relevance: Research has suggested that derivatives of 2-oxo-2-phenylacetaldehyde could exhibit biological activities, including antimicrobial properties, making it a compound of interest in medicinal chemistry.

In the words of a chemist, "The beauty of organic compounds lies in their ability to transform and contribute to the world around us." With its diverse applications and synthetic utility, 2-oxo-2-phenylacetaldehyde undoubtedly exemplifies this beauty.


Studying such compounds not only enhances our understanding of organic reactions but also paves the way for innovative solutions in various fields, including pharmaceuticals and materials science.

Synonyms
phenylglyoxal
2-oxo-2-phenylacetaldehyde
benzoylformaldehyde
phenylethanedione
benzoylcarboxaldehyde
glyoxal, phenyl-
alpha-oxobenzeneacetaldehyde
Benzeneacetaldehyde, .alpha.-oxo-
CCRIS 966
Benzeneacetaldehyde, alpha-oxo-
EINECS 214-036-1
NSC 26909
NSC 156299
UNII-N45G3015PA
BRN 1854721
DTXSID8025888
AI3-22132
benzeneacetaldehyde, alpha-oxo-, monohydrate
N45G3015PA
NSC-26909
1-PHENYLETHANEDIONE
NSC-156299
DTXCID705888
4-07-00-02129 (Beilstein Handbook Reference)
Benzeneacetaldehyde, alpha-oxo-(9CI)
ojugvdodnpjeec-uhfffaoysa-n
1074-12-0
Oxo(phenyl)acetaldehyde
Phenyl glyoxal
MFCD00006959
Oxo-phenyl-acetaldehyde
CHEBI:88868
NSC627436
2-oxo-2-phenyl-acetaldehyde
Benzoyl formaldehyde
a-hydroxy phenylketene
Phenylglyoxal treated BSA
Oxo(phenyl)acetaldehyde #
Phenylglyoxal treated casein
Benzeneacetaldehyde, a-oxo-
SCHEMBL57493
CHEMBL233632
NSC26909
Tox21_200277
MSK178335
NSC156299
AKOS009031532
AB00817
NSC-627436
NCGC00091619-01
NCGC00091619-02
NCGC00257831-01
AS-50086
SY047494
CAS-1074-12-0
DB-040753
NS00023460
P0652
EN300-33982
O10845
Q5934181
Z1954804411