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Ethyl benzoylacetate

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Identification
Molecular formula
C11H12O3
CAS number
94-02-0
IUPAC name
ethyl 3-oxo-3-phenyl-propanoate
State
State

At room temperature, ethyl benzoylacetate is a liquid. It is stable under normal conditions but may decompose upon heating or under the influence of strong acids or bases.

Melting point (Celsius)
-19.00
Melting point (Kelvin)
254.15
Boiling point (Celsius)
270.00
Boiling point (Kelvin)
543.15
General information
Molecular weight
192.20g/mol
Molar mass
192.2040g/mol
Density
1.1105g/cm3
Appearence

Ethyl benzoylacetate is typically a colorless to pale yellow liquid. It has a distinctive sweet, flowery odor reminiscent of hawthorn and may display a slightly viscous consistency. When exposed to air, it can undergo oxidation and acquire a darker hue.

Comment on solubility

Solubility of Ethyl 3-Oxo-3-phenyl-propanoate

Ethyl 3-oxo-3-phenyl-propanoate, a member of the ester family, presents intriguing solubility characteristics that are worthy of exploration. Its solubility can be influenced significantly by various factors, including:

  • Polarity: The presence of polar functional groups and the overall structure impact its ability to dissolve in different solvents.
  • Solvent Type: Typically, ethyl esters like this compound are more soluble in organic solvents (e.g., ethyl acetate, ethanol) than in water, due to their non-polar hydrocarbon chains.
  • Temperature: Increased temperature often enhances solubility, allowing for greater molecular movement and interaction with solvents.

It is essential to note that esters generally exhibit moderate to high solubility in organic solvents, while their solubility in water may be limited. As a general guideline:

  1. High solubility: In non-polar solvents.
  2. Moderate solubility: In polar organic solvents.
  3. Low solubility: In aqueous solutions.

As we reflect on its solubility characteristics, keep in mind the principle that "like dissolves like," which emphasizes the significance of molecular interactions in determining the solubility of chemical compounds.

Interesting facts

Exploring Ethyl 3-Oxo-3-Phenyl-Propanoate

Ethyl 3-oxo-3-phenyl-propanoate, often referred to in chemical discourse as a versatile compound, exhibits a wealth of interesting properties and applications in the realm of organic chemistry. This compound belongs to the family of α-keto esters, which are recognized for their significance in various synthetic pathways.

Interesting Facts

  • Synthesis: Ethyl 3-oxo-3-phenyl-propanoate can be synthesized through methods such as the Claisen condensation, allowing chemists to explore various routes for its preparation. This process serves as an excellent example of carbon-carbon bond formation in organic synthesis.
  • Reactivity: The presence of both an ester and a ketone group in its structure makes this compound a reactive intermediary. It can participate in various reactions, such as nucleophilic additions, which can lead to the formation of complex molecules.
  • Application in Synthesis: This compound is instrumental in the synthesis of larger, more complex organic molecules, especially in the pharmaceutical industry where it can serve as a building block for various medicinal compounds.
  • Flavors and Fragrances: Ethyl esters are well-known for their pleasant aroma, and while specific sensory data on this compound may be limited, compounds of similar structures are often utilized in the creation of flavoring agents and fragrances.
  • Chemical Rearrangements: The structural features of ethyl 3-oxo-3-phenyl-propanoate allow it to undergo intriguing chemical rearrangements, making it a subject of interest for studies on reaction mechanisms.

In summary, ethyl 3-oxo-3-phenyl-propanoate is not just another compound in the vast world of organic chemistry; it is a testament to the intricacies of molecular interactions and the creativity required in synthesis. As chemists continue to explore its potentials, this compound may reveal even more applications and insights into the nature of chemical reactivity.

Synonyms
ETHYL BENZOYLACETATE
Ethyl 3-oxo-3-phenylpropanoate
94-02-0
Ethyl benzoyl acetate
Benzoylacetic acid ethyl ester
Ethyl beta-oxobenzenepropanoate
Benzoylacetic acid, ethyl ester
Ethyl 3-phenyl-3-oxopropanoate
Benzenepropanoic acid, beta-oxo-, ethyl ester
Acetic acid, benzoyl-, ethyl ester
Ethyl 3-oxo-3-phenylpropionate
1-Ethoxy-3-phenylpropane-1,3-dione
FEMA No. 2423
UNII-K8CHJ4MKM0
K8CHJ4MKM0
EINECS 202-295-3
ethylbenzoyl acetate
MFCD00009196
NSC 227214
Benzenepropanoic acid, .beta.-oxo-, ethyl ester
BRN 0389944
DTXSID4047094
AI3-01353
NSC-6774
NSC-227214
3-oxo-3-phenyl-propionic acid ethyl ester
DTXCID2027094
Ethyl .beta.-oxobenzenepropanoate
ETHYL BENZOYLACETATE [MI]
3-OXO,3-PHENYL-PROPANOIC ACID,ETHYL ESTER
4-10-00-02756 (Beilstein Handbook Reference)
ETHYL BENZOYL ACETATE [FCC]
ethylbenzoylacetate
ETHYL BENZOYL ACETATE [FHFI]
3-oxo-3-phenylpropionic acid ethyl ester
3-OXO-3-PHENYLPROPANOIC ACID ETHYL ESTER
ethyl 2-benzoylacetate
Ethyl 3oxo3phenylpropanoate
Ethyl 3phenyl3oxopropanoate
Ethyl 3phenyl3oxopropionate
Ethyl benzoylacetate, 97%
Ethyl betaoxobenzenepropanoate
benzoyl-acetic acid-ethylester
1Ethoxy3phenylpropane1,3dione
SCHEMBL124577
benzoyl acetic acid ethyl ester
ethyl 3-phenyl-3-oxopropionate
CHEMBL3182719
Ethyl betaketobetaphenylpropionate
FEMA 2423
NSC6774
CHEBI:173927
Acetic acid, benzoyl, ethyl ester
Ethyl 3-oxo-3-phenylpropanoate #
ethyl 3-phenyl-beta-ketopropanoate
HMS1789K04
ALBB-010188
STR00545
Tox21_302326
BBL027743
NSC227214
STK499920
AKOS000119880
betaOxobenzenepropanoic acid ethyl ester
CS-W007617
FE01440
CAS-94-02-0
s12382
NCGC00256276-01
AC-14224
SY003149
Benzenepropanoic acid, betaoxo, ethyl ester
DB-010078
Ethyl benzoylacetate, technical grade, 90%
B0097
NS00012374
EN300-17880
Ethyl benzoylacetate, technical, >=95% (HPLC)
Ethyl benzoylacetate, Lonza quality, >=98% (GC)
Ethyl benzoylacetate, redist., >=97.0% (HPLC)
Ethyl benzoylacetate, Lonza quality, >=91.0% (GC)
Q27282091
Z57055787
F0787-0004