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Phenyl 2,2-dimethylpropanoate

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Identification
Molecular formula
C11H14O2
CAS number
7477-98-1
IUPAC name
phenyl 2,2-dimethylpropanoate
State
State

This compound is a liquid at room temperature.

Melting point (Celsius)
-30.00
Melting point (Kelvin)
243.20
Boiling point (Celsius)
195.00
Boiling point (Kelvin)
468.00
General information
Molecular weight
178.24g/mol
Molar mass
178.2430g/mol
Density
0.9997g/cm3
Appearence

Phenyl 2,2-dimethylpropanoate is typically a colorless liquid. It may have a characteristic ester-like odor, which can be described as sweet and fruity.

Comment on solubility

Solubility of Phenyl 2,2-Dimethylpropanoate

Pheynl 2,2-dimethylpropanoate is an organic compound that exhibits some notable solubility characteristics. Generally, its solubility can be influenced by various factors including temperature and the chemical environment. Here are some important points regarding its solubility:

  • In Non-Polar Solvents: Phenyl 2,2-dimethylpropanoate is typically more soluble in non-polar solvents such as hexane or toluene. This is due to its hydrocarbon structure which does not interact well with polar solvents.
  • In Polar Solvents: Its solubility in polar solvents like water is quite limited. This is attributed to the absence of functional groups capable of forming strong hydrogen bonds with water molecules.
  • Temperature Dependency: The solubility of phenyl 2,2-dimethylpropanoate may increase with rising temperatures, following the general trend observed with organic compounds. This behavior is useful in processes requiring dissolution or extraction.

In essence, when assessing the solubility of phenyl 2,2-dimethylpropanoate, one should keep in mind the type of solvent and temperature conditions. As stated, it is best suited to non-polar environments, highlighting the importance of considering solvent compatibility in applications.

Interesting facts

Interesting Facts about Phenyl 2,2-Dimethylpropanoate

Pheynl 2,2-dimethylpropanoate is an intriguing compound within the realm of organic chemistry, primarily known for its versatile applications and structural uniqueness. Here are some fascinating insights about this compound:

  • Functional Groups: This compound belongs to the ester functional group family, characterized by its ability to form through esterification reactions. Esters are significant due to their fragrant properties, often resembling fruity scents.
  • Synthetic Utility: Phenyl 2,2-dimethylpropanoate is frequently used as an intermediate in various chemical syntheses. The presence of both the aromatic phenyl group and the branched hydrocarbon chain provides unique reactivity, making it a valuable building block in organic synthesis.
  • Flavors and Fragrances: Given its ester format, it is often utilized in the creation of various flavors and fragrances. Its unique structure allows it to contribute distinctive notes in perfumes and food industries.
  • Biological Relevance: Esters, including phenyl 2,2-dimethylpropanoate, are often studied for their roles in biological systems. They can act as metabolites or signaling molecules, influencing various biochemical pathways.
  • Environmental Consideration: As with many organic compounds, the environmental impact of such esters warrants attention. Researchers are actively studying their biodegradability and long-term effects on ecosystems.

In the words of chemists, "the beauty of organic chemistry is in the diversity of compounds and their multifaceted applications." Phenyl 2,2-dimethylpropanoate exemplifies this diversity, showcasing how a single molecule can play multiple roles across industries.

Synonyms
Pivalic acid, phenyl ester
4920-92-7
Phenyl pivalate
Phenyl trimethylacetate
PHENYL 2,2-DIMETHYLPROPANOATE
2,2-Dimethylpropanoic acid, phenyl ester
2,2-dimethyl-propionic acid phenyl ester
Propanoic acid, 2,2-dimethyl-, phenyl ester
SCHEMBL2342588
DTXSID40197721
PUXKSJCSTXMIKR-UHFFFAOYSA-N
NSC74550
NSC 74550
NSC-74550
AKOS002943606
Propanoic acid,2-dimethyl-, phenyl ester