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Mandelic Acid Phenyl Ester

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Identification
Molecular formula
C16H14O3
CAS number
4360-12-7
IUPAC name
phenyl 2-hydroxy-2-phenyl-propanoate
State
State

At room temperature, this compound is typically in a liquid state, which may solidify around 30 °C.

Melting point (Celsius)
30.00
Melting point (Kelvin)
303.15
Boiling point (Celsius)
290.00
Boiling point (Kelvin)
563.15
General information
Molecular weight
212.24g/mol
Molar mass
212.2400g/mol
Density
1.1580g/cm3
Appearence

Mandelic acid phenyl ester appears as a colorless to pale yellow liquid. It may exhibit a mild aromatic odor characteristic of phenyl esters.

Comment on solubility

Solubility of Phenyl 2-hydroxy-2-phenyl-propanoate

Pheynl 2-hydroxy-2-phenyl-propanoate, commonly referred to as a phenolic ester, is known for its intriguing solubility characteristics. Its solubility is influenced by several factors, making it a compound of interest in various chemical applications.

Key Solubility Factors

  • Polarity: The presence of hydroxyl groups contributes to the molecule's polarity, aiding in solubility in polar solvents like water to some extent.
  • Aromatic Structure: The phenolic rings enhance interactions with organic solvents, rendering the compound more soluble in non-polar or weakly polar solvents such as hexane or toluene.
  • Temperature: Increased temperature usually improves solubility. Therefore, the solubility of phenyl 2-hydroxy-2-phenyl-propanoate can be enhanced at elevated temperatures.

In summary, this compound showcases dual solubility potential, demonstrating compatibility with both polar and non-polar environments, but its solubility in water is relatively limited. As stated, "the solubility profile is essential for practical applications," highlighting the significance of its understanding in the realms of pharmaceuticals and organic syntheses.

Interesting facts

Interesting Facts about Phenyl 2-Hydroxy-2-Phenyl-Propanoate

Pheynl 2-hydroxy-2-phenyl-propanoate, also known as phenyl glycidate, is a fascinating compound that features prominently in various scientific domains. Here are some intriguing insights about this compound:

  • Functional Group Diversity: The compound contains multiple functional groups, including both phenol and ester groups, which contribute to its reactivity and potential application in organic synthesis.
  • Applications in Synthesis: Often utilized as a reagent in synthetic organic chemistry, it serves as a key intermediate for synthesizing diverse pharmaceutical compounds, fragrances, and flavoring agents.
  • Biological Activity: Research shows that phenyl glycidate exhibits biological activities, making it a potential candidate for pharmacological research and development, specifically in drug discovery.
  • Flavor and Fragrance: Due to its aromatic properties, it has been explored in the formulation of food additives, contributing to the flavor and scent profile of various products.
  • Intriguing History: The compound's discovery and subsequent studies reflect the evolution of organic chemistry and the importance of esters in chemical processes over the decades.

As a compound with rich applications and intriguing properties, phenyl 2-hydroxy-2-phenyl-propanoate continues to inspire scientific inquiry. Its multifaceted nature makes it a topic of interest for chemists, biologists, and industry professionals alike.


Synonyms
Methyl-4-phenylmandelic acid
6244-54-8
alpha-Methyl-4-phenylmandelic acid
BRN 2649668
MANDELIC ACID, alpha-METHYL-4-PHENYL-
3-10-00-01200 (Beilstein Handbook Reference)
phenyl 2-hydroxy-2-phenylpropanoate
DTXSID90978007