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Propyl 5-nitrofuran-2-carboxylate

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Identification
Molecular formula
C8H9NO5
CAS number
19241-82-4
IUPAC name
propyl 5-nitrofuran-2-carboxylate
State
State

At room temperature, Propyl 5-nitrofuran-2-carboxylate is in a solid state, characterized by its crystalline form.

Melting point (Celsius)
91.00
Melting point (Kelvin)
364.15
Boiling point (Celsius)
276.00
Boiling point (Kelvin)
549.15
General information
Molecular weight
211.19g/mol
Molar mass
211.1850g/mol
Density
1.2900g/cm3
Appearence

Propyl 5-nitrofuran-2-carboxylate typically appears as a crystalline solid. The crystals can be slightly yellow due to the nitro group present in the structure.

Comment on solubility

Solubility of Propyl 5-Nitrofuran-2-Carboxylate

Propyl 5-nitrofuran-2-carboxylate, a compound with the formula C10H10N2O4, exhibits notable solubility characteristics that are influenced by its molecular structure. Here are some insights into its solubility:

  • Polarity: The presence of the nitro group and the carboxylate moiety contributes to the polarity of the molecule, enhancing its interaction with polar solvents.
  • Solvent Compatibility: Propyl 5-nitrofuran-2-carboxylate is generally soluble in:
    • Organic solvents such as ethanol, methanol, and acetone.
    • Less soluble in non-polar solvents, which indicates its polar characteristics.
  • Temperature Influence: Like many organic compounds, solubility may increase with rising temperatures, promoting dissolution in various solvents.
  • Applications: The solubility of this compound in polar solvents makes it useful in various applications including organic synthesis and pharmaceuticals.

In conclusion, the solubility of propyl 5-nitrofuran-2-carboxylate is largely determined by its molecular features and the nature of the solvent used. This solubility profile allows for its diverse applications across different fields.

Interesting facts

Interesting Facts about Propyl 5-Nitrofuran-2-Carboxylate

Propyl 5-nitrofuran-2-carboxylate is a fascinating compound with a variety of applications in the field of chemistry and beyond. Here are some intriguing points about this compound:

  • Chemical Structure: The compound features a nitrofuran ring, which is known for its unique electronic properties. This structure can influence its reactivity and interactions with other chemical species.
  • Biological Activities: Compounds like propyl 5-nitrofuran-2-carboxylate are often studied for their potential biological activity. They may exhibit antibacterial or antifungal properties, making them of interest in medicinal chemistry.
  • Agrochemical Applications: This compound may serve as a precursor or key ingredient in agricultural chemicals, contributing to the development of new pesticides or herbicides.
  • Synthesis Route: The synthesis of propyl 5-nitrofuran-2-carboxylate can be achieved through various chemical reactions, often involving the modification of simpler furan derivatives, showcasing the versatility and creativity in synthetic organic chemistry.

“The beauty of organic chemistry lies in its intricate structures and the fascinating reactions that can occur.”

In summary, propyl 5-nitrofuran-2-carboxylate exemplifies the remarkable intersection of chemistry and its applications in real-world scenarios, highlighting the broader implications of studying such compounds.

Synonyms
n-Propyl-5-nitro-2-furoate
20001-36-9
2-FURANCARBOXYLIC ACID, 5-NITRO-, PROPYL ESTER
2-Nitrofuran-5-carboxylate propyl ester
NSC-74626
NSC 74626
BRN 1378786
2-Furoic acid, 5-nitro-, propyl ester
AI3-23600
NSC74626
NCIOpen2_000765
SCHEMBL27861614
DTXSID50173814
6CY6739G7S
AKOS008949522
DS-012095