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Identification
Molecular formula
C10H8N2O6
CAS number
742-30-3
IUPAC name
methyl 5-methyl-3-(5-nitro-2-furyl)isoxazole-4-carboxylate
State
State

At room temperature, this compound exists as a solid. It is usually handled in powdered form for use in various chemical applications.

Melting point (Celsius)
114.00
Melting point (Kelvin)
387.15
Boiling point (Celsius)
298.00
Boiling point (Kelvin)
571.15
General information
Molecular weight
252.18g/mol
Molar mass
252.1930g/mol
Density
1.4200g/cm3
Appearence

Methyl 5-methyl-3-(5-nitro-2-furyl)isoxazole-4-carboxylate appears as a yellow crystalline solid. It is sensitive to light and may degrade upon exposure, hence it is typically stored in a dark container.

Comment on solubility

Solubility of Methyl 5-methyl-3-(5-nitro-2-furyl)isoxazole-4-carboxylate

The solubility of methyl 5-methyl-3-(5-nitro-2-furyl)isoxazole-4-carboxylate can be described through several key points:

  • Polarity: As a compound featuring an isoxazole ring and nitro groups, its solubility can vary significantly with the solvent due to polarity. Nitro groups can enhance the solubility in polar solvents.
  • Solvent Compatibility: Typically, compounds with similar polarities are soluble in one another. Therefore, methyl 5-methyl-3-(5-nitro-2-furyl)isoxazole-4-carboxylate may demonstrate good solubility in polar solvents like water or ethanol, while being less soluble in non-polar solvents.
  • Temperature Effect: Solubility often increases with temperature. Higher temperatures can assist in increasing the kinetic energy of molecules, thus promoting dissolution.
  • Hydrogen Bonding: The presence of carboxylate groups may potentially form hydrogen bonds with polar solvents, enhancing solubility in appropriate environments.

In summary, while specific solubility data may vary, the overall nature of methyl 5-methyl-3-(5-nitro-2-furyl)isoxazole-4-carboxylate suggests that it has the potential for good solubility in polar solvents due to its structural features. It is essential to consider the solvent choice and environmental conditions when exploring its solubility properties further.

Interesting facts

Interesting Facts about Methyl 5-Methyl-3-(5-Nitro-2-Furyl)Isoxazole-4-Carboxylate

Methyl 5-methyl-3-(5-nitro-2-furyl)isoxazole-4-carboxylate, often referred to in the scientific community by its abbreviated name, exhibits a fascinating structure and a variety of potential applications. Here are some intriguing aspects of this compound:

  • Unique Functional Groups: This compound incorporates both isoxazole and nitro functionalities, which are pivotal in medicinal chemistry and the development of pharmaceuticals.
  • Potential Applications: Due to its structure, it may serve as a precursor in the synthesis of biologically active compounds, especially in drug discovery.
  • Pharmacological Activities: Compounds containing isoxazole rings are often investigated for anti-inflammatory, antibacterial, and antifungal properties, making this compound a topic of interest for researchers.
  • Structure-Activity Relationship (SAR): The substitution pattern on the isoxazole ring and the presence of the nitro group allow scientists to explore the effects of these modifications on the compound's biological activity.

In the words of renowned chemists, "Understanding the intricacies of molecular structures leads us down the path of innovative drug design." Through exploring compounds like methyl 5-methyl-3-(5-nitro-2-furyl)isoxazole-4-carboxylate, we delve into the vibrant world of organic chemistry, where each molecule has the potential to make significant contributions to science and medicine.

As ongoing research continues to uncover its full potential, this compound represents yet another exciting frontier in the ever-evolving field of chemical sciences.

Synonyms
BRN 0621304
4-ISOXAZOLECARBOXYLIC ACID, 5-METHYL-3-(5-NITRO-2-FURYL)-, METHYL ESTER
17960-17-7
DTXSID60170839
5-Methyl-3-(5-nitro-2-furyl)-4-isoxazolecarboxylic acid methyl ester
DTXCID6093330