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Ethyl furan-2-carboxylate

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Identification
Molecular formula
C7H8O3
CAS number
614-99-3
IUPAC name
ethyl furan-2-carboxylate
State
State

Ethyl furan-2-carboxylate is typically found in a liquid state at room temperature.

Melting point (Celsius)
-31.00
Melting point (Kelvin)
242.00
Boiling point (Celsius)
204.00
Boiling point (Kelvin)
477.00
General information
Molecular weight
154.14g/mol
Molar mass
154.1720g/mol
Density
1.0845g/cm3
Appearence

Ethyl furan-2-carboxylate is a colorless to pale yellow liquid with a sweet odor. It is generally clear and transparent in appearance.

Comment on solubility

Solubility of Ethyl Furan-2-carboxylate

Ethyl furan-2-carboxylate is a fascinating compound known for its specific solubility characteristics. Generally, the solubility of this compound in various solvents can be influenced by several factors:

  • Polarity: Ethyl furan-2-carboxylate is a moderately polar compound due to the presence of the carboxylate group which can engage in hydrogen bonding.
  • Solvent type: This compound exhibits good solubility in polar organic solvents such as:
    • Ethyl alcohol
    • Acetone
    • DMSO (Dimethyl sulfoxide)
    • Acetonitrile
  • Water solubility: While ethyl furan-2-carboxylate is generally not soluble in water, its solubility may slightly increase with temperature due to the increased kinetic energy which allows for more interactions.

In summary, the solubility profile of ethyl furan-2-carboxylate is significantly affected by its molecular structure and environmental conditions. It is most soluble in polar organic solvents, which can enhance its reactivity in various chemical applications.

Interesting facts

Interesting Facts about Ethyl Furan-2-Carboxylate

Ethyl furan-2-carboxylate is a fascinating compound that belongs to the family of furan derivatives, which are known for their distinctive aromatic properties. Below are some key insights into this intriguing compound:

  • Structural Significance: Ethyl furan-2-carboxylate features a furan ring, a five-membered heterocyclic structure that contains both carbon and oxygen atoms. This unique structure contributes to its reactivity and the types of chemical reactions it can undergo.
  • Applications: Due to its versatile structure, ethyl furan-2-carboxylate finds use in various fields such as organic synthesis, pharmaceuticals, and the development of fragrances. It plays a role in the creation of compounds that can be used in drug design.
  • Synthesis: This compound can be synthesized through different methods, typically involving the condensation of furan derivatives with carboxylic acids or their derivatives, showcasing the importance of furan in synthetic organic chemistry.
  • Reactivity: The presence of both a furan ring and an ester functional group makes ethyl furan-2-carboxylate a rich site for nucleophilic attack, which opens pathways for further chemical transformations, potentially leading to the formation of more complex structures.
  • Biological Activity: Some studies have suggested that derivatives of this compound may exhibit biological activity, indicating potential avenues for research into new therapeutic agents.

As a compound of interest in both academic and industrial research, ethyl furan-2-carboxylate is not just a molecule; it's a gateway to exploring the larger realm of furan chemistry and its implications in the world of science. Remember, every time you examine a compound, you are not merely looking at a chemical; you are engaging with a story of discovery and innovation!

Synonyms
ETHYL 2-FUROATE
Ethyl furan-2-carboxylate
614-99-3
Ethyl 2-furancarboxylate
2-Furancarboxylic acid, ethyl ester
Ethyl-2-furoate
Ethyl pyromucate
2-Carboethoxyfuran
Ethyl 2-furylcarboxylate
2-(Ethoxycarbonyl)furan
NSC 2304
2-Furoic Acid Ethyl Ester
EINECS 210-404-0
BRN 0002653
AI3-23056
S1H449R92T
NSC-2304
DTXSID0060640
2-FUROIC ACID ETHYL ESTER [MI]
DTXCID2043032
210-404-0
Ethyl furoate
1335-40-6
Ethyl2-furoate
Furan-2-carboxylic acid ethyl ester
2-Furoic acid, ethyl ester
Furancarboxylic acid, ethyl ester
MFCD00003237
Furoic acid, ethyl ester
UNII-31OM7UT24E
UNII-S1H449R92T
2-Furancarboxylic Acid Ethyl Ester
EINECS 215-631-9
ethyl uran-2-carboxylate
Ethyl 2-furoate, 99%
WLN: T5OJ BVO2
SCHEMBL859237
31OM7UT24E
CHEMBL4634762
NSC2304
CHEBI:169174
Ethyl 2-furoate, >=98%, FG
BBL001830
STK037149
AKOS000119259
FE70446
AS-14743
BP-13163
SY013608
DB-003644
DB-297597
CS-0015334
F0098
NS00022502
EN300-16109
H11621
Q27288446
Z54848724
F0001-1621
InChI=1/C7H8O3/c1-2-9-7(8)6-4-3-5-10-6/h3-5H,2H2,1H