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Benzoylacetone

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Identification
Molecular formula
C10H10O3
CAS number
93-91-4
IUPAC name
(1-acetyl-2-oxo-propyl) benzoate
State
State

At room temperature, benzoylacetone appears as a solid, typically in crystalline form.

Melting point (Celsius)
39.00
Melting point (Kelvin)
312.15
Boiling point (Celsius)
281.00
Boiling point (Kelvin)
554.15
General information
Molecular weight
176.18g/mol
Molar mass
176.1840g/mol
Density
1.0990g/cm3
Appearence

Benzoylacetone is typically a yellow crystalline substance.

Comment on solubility

Solubility of (1-acetyl-2-oxo-propyl) benzoate

(1-acetyl-2-oxo-propyl) benzoate presents interesting characteristics regarding its solubility. Generally, the solubility of this compound is influenced by several factors:

  • Polarity: The presence of both polar (carbonyl groups) and non-polar (benzoate group) functional groups leads to mixed solubility characteristics.
  • Solvent Interaction: It is typically more soluble in organic solvents like ethanol and acetone, which can stabilize the polar interactions present in the molecule.
  • Temperature Dependence: Solubility may increase with temperature, which is a common trend in organic compounds.
  • pH Effect: The solubility can also be affected by the pH of the solution, potentially altering ionization states.

As a result, one might observe that:

  • In polar solvents, there is likely moderate solubility due to hydrogen bonding capabilities.
  • In non-polar solvents, solubility may be significantly reduced due to lack of favorable interactions.

In conclusion, (1-acetyl-2-oxo-propyl) benzoate showcases variable solubility influenced by solvent choice and environmental conditions, making it essential to consider these factors when predicting its behavior in practical applications.

Interesting facts

Exploring (1-acetyl-2-oxo-propyl) benzoate

(1-acetyl-2-oxo-propyl) benzoate is a fascinating compound known for its unique properties and applications. As a member of the ester family, it showcases the beauty of organic synthesis.

Key Attributes

  • Versatile Reactivity: This compound can serve as a precursor in various organic reactions, enabling chemists to construct complex molecules.
  • Flavor and Fragrance: Esters like (1-acetyl-2-oxo-propyl) benzoate often play a role in the creation of synthetic flavors and fragrances, adding delightful aromas to products.
  • Pharmaceutical Applications: Its derivatives are explored in medicinal chemistry, offering potential therapeutic benefits.

One interesting aspect of (1-acetyl-2-oxo-propyl) benzoate is its role in biochemistry. Compounds similar to this one can mimic natural substances, influencing metabolic pathways and leading to innovative drug design.

Usage in Research

In laboratory settings, this compound can be a subject of study due to its intriguing molecular structure. Researchers often utilize it to:

  1. Investigate reaction mechanisms
  2. Discover new synthetic pathways
  3. Enhance understanding of ester interactions

Furthermore, the ability to tailor the synthesis of (1-acetyl-2-oxo-propyl) benzoate demonstrates the art of organic chemistry, where slight modifications can lead to entirely different chemical behaviors. As one chemist noted, "The magic of chemistry lies in the transformation from simple molecules to complex wonders."

In conclusion, (1-acetyl-2-oxo-propyl) benzoate is not just a compound, but a key to unlocking the intricate world of organic synthesis and the extensive potential it holds across various industries.

Synonyms
2,4-dioxopentan-3-yl benzoate
4620-47-7
3-(BENZOYLOXY)-2,4-PENTANEDIONE
NSC58119
2, 3-(benzoyloxy)-
2, 3-hydroxy-, benzoate
1-acetyl-2-oxopropyl benzoate
3-benzoyloxy-2,4-pentanedione
SCHEMBL2659176
3-benzoyloxy-2,4-pentane-dione
DTXSID80196773
VWWVUXIKLRIRAZ-UHFFFAOYSA-N
NSC 58119
NSC-58119
benzoic acid 1-acetyl-2-oxo-propyl ester
DS-003609