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Methyl furan-2-carboxylate

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Identification
Molecular formula
C6H6O3
CAS number
4540-31-0
IUPAC name
methyl furan-2-carboxylate
State
State

At room temperature, methyl furan-2-carboxylate is a liquid.

Melting point (Celsius)
-62.00
Melting point (Kelvin)
211.00
Boiling point (Celsius)
196.00
Boiling point (Kelvin)
469.00
General information
Molecular weight
126.11g/mol
Molar mass
126.1110g/mol
Density
1.1100g/cm3
Appearence

Methyl furan-2-carboxylate is a colorless to pale yellow liquid with a characteristic fruity odor.

Comment on solubility

Solubility of Methyl Furan-2-carboxylate

Methyl furan-2-carboxylate is a compound that displays interesting solubility characteristics. As with many esters, its solubility depends on the solvent used and its molecular structure. Here are some key points regarding its solubility:

  • Polar solvents: Methyl furan-2-carboxylate is expected to be soluble in polar solvents like water due to the presence of its carboxylate functional group.
  • Non-polar solvents: This compound is also likely to display good solubility in non-polar organic solvents, such as hexane and ether, attributed to its relatively hydrophobic furan ring.
  • Temperature dependency: Its solubility can increase with temperature, which is a common phenomenon for many organic compounds.
  • pH sensitivity: The solubility may also vary with pH, especially as the carboxylate group can engage in protonation/deprotonation under different pH conditions.

Overall, due to its unique structure, methyl furan-2-carboxylate exhibits a dual solubility profile, allowing it to dissolve effectively in both polar and non-polar environments. This makes it quite versatile in various chemical applications.

Interesting facts

Interesting Facts about Methyl furan-2-carboxylate

Methyl furan-2-carboxylate is a fascinating organic compound that showcases the intricacies of functionalized furan derivatives. Here are some engaging insights about this compound:

  • Structural Significance: The compound features a furan ring, which is characterized by its five-membered aromatic structure. This ring plays a pivotal role in the compound's reactivity and stability.
  • Reactivity: Methyl furan-2-carboxylate is known for its versatile reactivity, often participating in various chemical reactions such as esterification and Michael additions.
  • Synthetic Utility: The compound serves as an important precursor in organic synthesis, particularly in the manufacture of bioactive molecules and pharmaceuticals.
  • Natural Occurrence: Interestingly, certain furan derivatives, including methyl furan-2-carboxylate, can be found in natural products, serving as flavoring agents or indicators of biochemical pathways in various organisms.
  • Green Chemistry: Its application in the synthesis of biofuels and other renewable resources highlights its significance in the context of green chemistry, promoting sustainability in chemical processes.

In summary, methyl furan-2-carboxylate is not just an ordinary compound; it embodies the wonders of organic chemistry, bridging the gap between synthetic applications and natural occurrences. As a chemistry enthusiast or scientist, delving into the properties and potentials of this compound can lead to remarkable discoveries!

Synonyms
Methyl 2-furoate
Methyl furan-2-carboxylate
611-13-2
Methyl pyromucate
Methyl 2-furancarboxylate
METHYL FUROATE
2-Furancarboxylic acid, methyl ester
2-(Methoxycarbonyl)furan
Pyromucic acid methyl ester
2-FUROIC ACID, METHYL ESTER
Methyl 2-furylcarboxylate
2-Furancarboxylic Acid Methyl Ester
FEMA No. 2703
NSC 35551
CCRIS 2158
UNII-O9A8D29YDE
EINECS 210-254-6
O9A8D29YDE
Methyl alpha-furoate
BRN 0111110
AI3-23585
METHYL2-FUROATE
Methyl .alpha.-furoate
NSC-35551
METHYL FUROATE [FCC]
METHYL FUROATE [FHFI]
METHYL 2-FUROATE [MI]
DTXSID7060598
5-18-06-00103 (Beilstein Handbook Reference)
Furan-alpha-carboxylic acid methyl ester
Furan-.alpha.-carboxylic acid methyl ester
DTXCID9042962
210-254-6
hdjlsecjeqspkw-uhfffaoysa-n
Furoic acid, methyl ester
Furancarboxylic acid, methyl ester
2-Furoic acid methyl ester
MFCD00003236
METHYL-2-FUROATE
furan-2-carboxylic acid methyl ester
AH 22254X; Fluticasone furoate related; Methyl 2-furoate
2-methyl furate
Methyl 2-furoate ,
Furoic acid methyl ester
Methylfuran-2-carboxylate
methyl uran-2-carboxylate
Methyl 2-furoate, 98%
WLN: T5OJ BVO1
SCHEMBL363937
FEMA 2703
CHEBI:167081
Methyl 2-furoate, >=98%, FG
HY-Y0949
NSC35551
2-furan carboxylic acid methyl ester
s5636
STK397389
AKOS000120062
CCG-266097
CS-W020101
FM14749
Methyl 2-furoate, natural, 99%, FG
AS-14803
DB-003714
F0075
NS00012896
EN300-15493
D78223
Q22083556
Z19719727
F0001-1604