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
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:
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.