Skip to main content

Ethyl 3-phenyloxirane-2-carboxylate

ADVERTISEMENT
Identification
Molecular formula
C11H12O3
CAS number
7351-48-8
IUPAC name
ethyl 3-phenyloxirane-2-carboxylate
State
State

At room temperature, ethyl 3-phenyloxirane-2-carboxylate is typically found in a liquid state.

Melting point (Celsius)
-56.00
Melting point (Kelvin)
217.00
Boiling point (Celsius)
273.00
Boiling point (Kelvin)
546.00
General information
Molecular weight
192.21g/mol
Molar mass
192.2120g/mol
Density
0.9721g/cm3
Appearence

Ethyl 3-phenyloxirane-2-carboxylate is a colorless liquid with a slightly yellowish tinge. It has a characteristic aromatic odor.

Comment on solubility

Solubility of Ethyl 3-phenyloxirane-2-carboxylate

Ethyl 3-phenyloxirane-2-carboxylate exhibits intriguing solubility characteristics that can be influenced by various factors. This compound, like many others in organic chemistry, displays different solubility profiles depending on the solvent used. Generally, the key points regarding its solubility are:

  • Polar solvents: Ethyl 3-phenyloxirane-2-carboxylate is likely to be more soluble in polar solvents such as water or alcohols due to the presence of the carboxylate functionality.
  • Nonpolar solvents: Its solubility in nonpolar solvents may be limited owing to the polar nature of the epoxide and carboxylate groups.
  • Temperature effects: As with many chemical compounds, an increase in temperature can enhance solubility, facilitating molecular interactions in the solvent phase.

As stated, "like dissolves like," meaning that polar compounds generally dissolve well in polar solvents while nonpolar compounds prefer nonpolar environments. Therefore, understanding the solubility of ethyl 3-phenyloxirane-2-carboxylate is crucial for its applications in fields such as organic synthesis and pharmaceuticals, where solvent choice can significantly influence reaction outcomes.

Interesting facts

Interesting Facts about Ethyl 3-Phenyloxirane-2-carboxylate

Ethyl 3-phenyloxirane-2-carboxylate is a fascinating compound in the realm of organic chemistry due to its unique structure and reactivity. Here are some engaging insights about this compound:

  • Structural Significance: The presence of an oxirane ring in its structure highlights the compound’s potential for undergoing epoxide reactions, which can lead to the formation of various valuable derivatives.
  • Reactivity: The compound is known for its ability to participate in nucleophilic ring-opening reactions, making it a useful intermediate for synthesizing complex organic molecules.
  • Applications: Ethyl 3-phenyloxirane-2-carboxylate is of interest in the pharmaceutical industry for its potential use in developing drug molecules due to the oxirane group's reactivity, allowing for modifications that improve biological activity.
  • Flavor and Fragrance Industries: Compounds like this can also serve as building blocks for creating flavors and fragrances, contributing to the development of diverse products in consumer goods.
  • Importance of Carboxylate Group: The carboxylate moiety in the compound enhances its solubility in polar solvents, broadening the scope of its applications in various chemical reactions.

Overall, ethyl 3-phenyloxirane-2-carboxylate serves as a prime example of how organic compounds can be pivotal in both academic research and industrial applications. As with many compounds in organic chemistry, its intriguing properties continue to captivate scientists, pushing the boundaries of what is possible in synthetic methodologies.

Synonyms
Ethyl 3-phenylglycidate
121-39-1
Ethyl 3-phenyloxirane-2-carboxylate
Ethyl phenylglycidate
Oxiranecarboxylic acid, 3-phenyl-, ethyl ester
ETHYL 2,3-EPOXY-3-PHENYLPROPIONATE
strawberry glycidate 2
Ethyl 3-phenyloxiranecarboxylate
Glycidic acid, 3-phenyl-, ethyl ester
2-Ethyl-3-phenylglycidate
3-Phenylglycidic acid, ethyl ester
Ethyl 3-phenyl-2,3-epoxypropionate
FEMA No. 2454
CCRIS 2623
HSDB 5404
UNII-2VVS520ZWM
NSC 8899
EINECS 204-467-3
BRN 0163394
DTXSID8025886
AI3-07356
NSC-8899
MFCD00005123
2VVS520ZWM
DTXCID905886
ETHYL PHENYLGLYCIDATE [FCC]
2-Oxiranecarboxylic acid, 3-phenyl-, ethyl ester
5-18-06-00373 (Beilstein Handbook Reference)
ETHYL 3-PHENYLGLYCIDATE [FHFI]
(+/-)-ETHYL 3-PHENYLGLYCIDATE
Ethyl .alpha.,.beta.-epoxyhydrocinnamate
ETHYL 3-PHENYLGLYCIDATE, (+/-)-
ethyl (2R,3S)-3-phenyloxirane-2-carboxylate
ETHYL 2,3-EPOXY-3-PHENYLPROPIONATE [HSDB]
ETHYL .ALPHA.,.BETA.-EPOXY-.BETA.-PHENYLPROPIONATE
CAS-121-39-1
ethyl (2R,3R)-3-phenyloxirane-2-carboxylate
Ethyl alpha,beta-epoxyhydrocinnamate
Ethyl 3-phenyl-2-oxiranecarboxylate
3-EPG
Ethyl alpha,beta-epoxy-alpha-phenylpropionate
126060-73-9
2272-55-1
(2R,3S)-Ethyl 3-phenyloxirane-2-carboxylate
Ethyl 3phenylglycidate
ethyl-3-phenylglycidate
3-phenyloxirane-2-carboxylic acid ethyl ester
Glycidic acid, ethyl ester
NCIOpen2_001041
SCHEMBL111475
Ethyl 3phenyloxiranecarboxylate
Ethyl 3phenyl2,3epoxypropionate
CHEMBL1369819
FEMA 2454
NSC8899
CHEBI:173922
Ethyl alpha,betaepoxyhydrocinnamate
3-Phenylglycidic Acid Ethyl Ester
Aldehyde C16 special (misleading)
Tox21_202247
Tox21_303367
Glycidic acid, 3phenyl, ethyl ester
AKOS000119937
Ethyl 3-phenyl-2-oxiranecarboxylate #
Ethyl alpha,betaepoxyalphaphenylpropionate
NCGC00091085-01
NCGC00091085-02
NCGC00257289-01
NCGC00259796-01
SY049268
DB-319427
CS-0075541
E0798
NS00012456
Oxiranecarboxylic acid, 3phenyl, ethyl ester
ETHYL 3-PHENYLGLYCIDATE, CIS + TRANS
3-phenyl-oxirane-2-carboxylic acid ethyl ester
D90572
3-PHENYL-OXIRANECARBOXYLIC ACID ETHYL ESTER
Ethyl 3-phenylglycidate, cis- and trans- mixture
Ethyl .alpha.,.beta.-epoxy-.alpha.-phenylpropionate
ETHYL ALPHA,BETA-EPOXY-BETA-PHENYLPROPIONATE
Q27255668
F0001-0342
Z104478934
54276-44-7