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2,3-Diphenylpropanoic acid

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Identification
Molecular formula
C15H14O2
CAS number
16648-65-0
IUPAC name
2,3-diphenylpropanoic acid
State
State

At room temperature, 2,3-Diphenylpropanoic acid is in a solid state. It is typically available as a powder or crystalline solid.

Melting point (Celsius)
154.00
Melting point (Kelvin)
427.00
Boiling point (Celsius)
374.90
Boiling point (Kelvin)
648.10
General information
Molecular weight
226.27g/mol
Molar mass
226.2740g/mol
Density
1.1565g/cm3
Appearence

2,3-Diphenylpropanoic acid is a white to off-white crystalline solid. The crystals are often needle-like or exhibit a granular structure depending on the conditions of crystallization.

Comment on solubility

Solubility of 2,3-Diphenylpropanoic Acid

2,3-Diphenylpropanoic acid, with the chemical formula C15H14O2, exhibits interesting solubility characteristics that are important for its applications in various chemical processes. Understanding its solubility can guide its use in organic synthesis and other fields.

Key solubility points:

  • Alcohols and Ethers: This compound is generally soluble in organic solvents such as alcohols and ethers due to its hydrophobic phenyl groups.
  • Water: The solubility in water is limited. This can be attributed to the relatively large molecular structure and the presence of phenyl groups that decrease its affinity for polar solvents.
  • pH Dependence: Solubility may vary with pH; in acidic or basic conditions, the ionization of the carboxylic acid group may enhance solubility in polar solvents.

Overall, while 2,3-diphenylpropanoic acid shows some degree of solubility in organic solvents, its solubility in water is markedly low. Thus, chemistry enthusiasts and researchers should keep these factors in mind when handling and utilizing this compound.

Interesting facts

Interesting Facts about 2,3-diphenylpropanoic acid

2,3-diphenylpropanoic acid is a fascinating compound that highlights the beauty of organic chemistry and the versatility of carboxylic acids. This particular acid features two phenyl groups attached to a three-carbon chain, imparting unique properties and functionalities. Here are some intriguing aspects of this compound:

  • Structural Diversity: The presence of multiple phenyl rings allows for a variety of steric and electronic interactions, making it a subject of study in fields such as medicinal chemistry and materials science.
  • Synthetic Applications: 2,3-diphenylpropanoic acid can be employed in the synthesis of other complex molecules, acting as a key intermediate in organic reactions. This makes it a useful compound in pharmaceutical development.
  • Thermotropic Properties: Compounds containing aromatic rings often display interesting thermal behaviors, which can lead to applications in thermoresponsive materials and liquid crystal technologies.
  • Biological Significance: Some studies point to the potential biological activity of carboxylic acids, including anti-inflammatory and analgesic effects, making this compound an interesting candidate for further biological assessments.
  • Research Focus: Continuous research on 2,3-diphenylpropanoic acid allows scientists to explore its reactivity and interactions further, contributing to our understanding of complex organic reaction mechanisms.

As a compound, 2,3-diphenylpropanoic acid serves as a beautiful illustration of how simple structures can lead to complex applications, underscoring the importance of molecular design in the realm of chemical science.

Synonyms
2,3-diphenylpropanoic acid
2,3-Diphenylpropionic acid
EINECS 222-065-6
NSC 49
DTXSID801311088
NSC 11135
DTXCID901740913
222-065-6
3333-15-1
MFCD00044405
2,3-Diphenyl-Propionic Acid
2,3-diphenylpropanoicacid
Maybridge3_003394
NSC49
2,3-diphenyl-propanoic acid
Oprea1_394675
SCHEMBL67234
NSC-49
HMS1440K06
ALBB-024829
NSC11135
benzenepropanoic acid, alpha-phenyl-
NSC-11135
AKOS001584772
AKOS016038005
AB92818
CCG-253843
IDI1_014781
AS-47862
SY021701
DB-048385
D1790
EU-0000158
NS00049543
F16387
AE-641/00381051
SR-01000389475
SR-01000389475-1