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Methyl furan-3-carboxylate

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Identification
Molecular formula
C6H6O3
CAS number
2363-08-6
IUPAC name
methyl furan-3-carboxylate
State
State

At room temperature, methyl furan-3-carboxylate exists as a liquid.

Melting point (Celsius)
-25.00
Melting point (Kelvin)
248.15
Boiling point (Celsius)
185.00
Boiling point (Kelvin)
458.15
General information
Molecular weight
126.11g/mol
Molar mass
126.1100g/mol
Density
1.1550g/cm3
Appearence

Methyl furan-3-carboxylate is a clear to light yellow liquid.

Comment on solubility

Solubility of Methyl Furan-3-Carboxylate

Methyl furan-3-carboxylate is a relatively polar compound, which significantly influences its solubility in various solvents. Its solubility characteristics can be summarized as follows:

  • Water Solubility: Methyl furan-3-carboxylate exhibits limited solubility in water. This is mainly due to the hydrophobic furan ring that hinders extensive interactions with water molecules.
  • Organic Solvents: It shows good solubility in organic solvents such as ethanol, methanol, and dichloromethane. These solvents can effectively solvate the polar parts of the molecule, facilitating dissolution.
  • Temperature Dependence: Its solubility often increases with temperature, which is a common behavior in many organic compounds. Higher temperatures can disrupt intermolecular interactions, leading to greater solvation.

Overall, while the solubility of methyl furan-3-carboxylate in water may be restricted, its affinity towards non-polar and polar organic solvents underscores its versatility in various chemical applications. Being aware of these solubility characteristics is crucial for optimizing its use in synthesis and other chemical processes.

Interesting facts

Interesting Facts about Methyl Furan-3-Carboxylate

Methyl furan-3-carboxylate is a fascinating compound that belongs to the family of furan derivatives. Here are some intriguing aspects of this compound:

  • Unique Structure: Methyl furan-3-carboxylate features a distinctive five-membered aromatic ring, which contributes to its notable chemical behavior and interactions.
  • Flavor and Aroma: This compound is known for its sweet, caramel-like odor, making it particularly interesting in the flavor and fragrance industries.
  • Reactivity: Methyl furan-3-carboxylate can undergo various chemical reactions, including alkylation and condensation, due to the presence of both furan and carboxylate functionalities.
  • Applications: It has potential applications in the synthesis of biologically active compounds, including pharmaceuticals and agrochemicals. Researchers are actively exploring its utility in drug design.
  • Environmental Perspective: As a compound derived from renewable resources, its synthesis can be seen as an environmentally friendly alternative compared to traditional petrochemical products.

In summary, methyl furan-3-carboxylate not only exhibits interesting structural features but also offers useful applications across various sectors. As scientists and students delve deeper into its properties, the potential for innovative uses continues to expand.

Synonyms
methyl furan-3-carboxylate
Methyl 3-furoate
Methyl 3-furancarboxylate
3-(Methoxycarbonyl)furan
NSC-305748
UNII-V05P3H54N5
V05P3H54N5
NSC 305748
672-679-7
zkhqsqylkssyip-uhfffaoysa-n
13129-23-2
3-Furancarboxylic acid, methyl ester
3-Furancarboxylic Acid Methyl Ester
3-Furoic acid, methyl ester
1334-76-5
MFCD06203671
furan-3-carboxylic acid methyl ester
Methyl furancarboxylate
3-Furoic Acid Methyl Ester
methylfuran-3-carboxylate
UNII-WS10TS94NA
WS10TS94NA
SCHEMBL826948
DTXSID00871954
BCP22945
EINECS 215-614-6
GEO-03412
NSC305748
AKOS009099213
SB60958
AC-25742
LS-13123
SY038697
DB-042020
CS-0187526
F0468
NS00127226
EN300-61704
D90674
Q27291369