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Benzoin oxime

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Identification
Molecular formula
C14H13NO2
CAS number
574-66-3
IUPAC name
2-hydroxy-1,2-diphenyl-ethanone oxime
State
State

At room temperature, Benzoin oxime is typically found as a solid due to its crystalline nature.

Melting point (Celsius)
119.00
Melting point (Kelvin)
392.15
Boiling point (Celsius)
330.00
Boiling point (Kelvin)
603.15
General information
Molecular weight
227.26g/mol
Molar mass
227.2610g/mol
Density
0.9200g/cm3
Appearence

Benzoin oxime typically appears as a white to off-white crystalline powder. The crystals may appear slightly yellowish, depending on purity and specific conditions of the compound.

Comment on solubility

Solubility of 2-hydroxy-1,2-diphenyl-ethanone oxime

The solubility of 2-hydroxy-1,2-diphenyl-ethanone oxime can be an intriguing aspect worth exploring. This compound, noted for its unique structure, generally displays the following solubility characteristics:

  • Solvent Dependence: It is often found to be soluble in organic solvents such as alcohols and ethers.
  • Water Solubility: The solubility in water may be limited due to the hydrophobic nature of the diphenyl groups.
  • Temperature Influence: Increased temperature may enhance solubility in certain solvents, promoting better dissolution.

In summary, the solubility of 2-hydroxy-1,2-diphenyl-ethanone oxime is influenced by factors such as the choice of solvent, temperature, and the molecular structure's hydrophobic properties. As a rule of thumb, like dissolves like, so organic solvents typically yield better solubility for this compound compared to polar solvents like water. However, specific experimental conditions should always be tested to ascertain solubility under varying circumstances.

Interesting facts

Interesting Facts about 2-Hydroxy-1,2-diphenyl-ethanone oxime

2-Hydroxy-1,2-diphenyl-ethanone oxime, also known as dibenzoyl oxime, is a fascinating organic compound with several notable attributes. Here are some of the key points that make this compound intriguing:

  • Oxime Functional Group: This compound features an oxime functional group, characterized by the general formula R1R2C=NOH. Oximes are known for their versatility in organic synthesis, often used as intermediates in the production of pharmaceuticals and fine chemicals.
  • Versatile Use in Organic Chemistry: 2-Hydroxy-1,2-diphenyl-ethanone oxime acts as a chelating agent for transition metals, enhancing its applicability in coordination chemistry, where it forms stable complexes crucial in catalysis and material science.
  • Biological Relevance: Studies have shown that oxime derivatives can exhibit biological activity, such as antibacterial and antifungal properties. This prompts ongoing research into their therapeutic potential.
  • Synthesis and Reactivity: This compound can be synthesized through the reaction of the corresponding ketone with hydroxylamine. Its reactivity allows it to participate in various organic transformations, highlighting its significance in synthetic chemistry.
  • Presence in Natural Products: The structural motifs present in 2-hydroxy-1,2-diphenyl-ethanone oxime resemble those found in certain natural products, which may lead to discoveries related to natural product synthesis.

As a result of these attributes, 2-hydroxy-1,2-diphenyl-ethanone oxime holds a unique position in both academic research and industrial applications. Its diverse functionality exemplifies the importance of understanding and exploring complex organic compounds in the world of chemistry.

Synonyms
441-38-3
alpha-Benzoin oxime
2-Hydroxy-1,2-diphenylethanone oxime
Benzoin oxime
Ethanone, 2-hydroxy-1,2-diphenyl-, oxime
(Z)-benzoin oxime
DTXSID30883202
Benzoinoximkomplexe
CBDivE_013170
HMS2901D18
AKOS016038569
SY057032
1-hydroxy-2-hydroxyimino-1,2-diphenylethane
NS00080356
D88599