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6-Nitro-3-(4-pyridyl)chromen-2-one

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Identification
Molecular formula
C14H8N2O4
CAS number
760207-83-8
IUPAC name
6-nitro-3-(4-pyridyl)chromen-2-one
State
State

At room temperature, 6-Nitro-3-(4-pyridyl)chromen-2-one is a solid.

Melting point (Celsius)
228.00
Melting point (Kelvin)
501.15
Boiling point (Celsius)
365.00
Boiling point (Kelvin)
638.15
General information
Molecular weight
308.27g/mol
Molar mass
308.2670g/mol
Density
1.4600g/cm3
Appearence

6-Nitro-3-(4-pyridyl)chromen-2-one typically appears as a yellow crystalline powder.

Comment on solubility

Solubility of 6-nitro-3-(4-pyridyl)chromen-2-one

The solubility of 6-nitro-3-(4-pyridyl)chromen-2-one is an intriguing aspect of its chemical behavior, influenced by its unique structure. Generally, the solubility of a compound can be affected by several factors:

  • Polarity: Due to the presence of both nitro and pyridyl groups, this compound exhibits polar characteristics, which may enhance its solubility in polar solvents like water.
  • Hydrogen Bonding: The nitrogen in the pyridyl group can engage in hydrogen bonding, potentially increasing solubility in protic solvents.
  • Temperature: Like many organic compounds, solubility can variation with temperature; it may increase in higher temperatures.

However, the overall solubility is not extensively documented and can be variable. It is essential to consider that:

  • Experimental conditions such as pH and the presence of other ions can dramatically affect solubility.
  • Empirical studies may provide better insights into the solubility profile of this compound.

In summary, while 6-nitro-3-(4-pyridyl)chromen-2-one shows potential for solubility due to its polar functional groups, detailed empirical data is necessary to fully understand its solubility behavior in various solvents.

Interesting facts

Exploring 6-Nitro-3-(4-pyridyl)chromen-2-one

6-Nitro-3-(4-pyridyl)chromen-2-one is a fascinating compound that lies at the intersection of organic chemistry and medicinal applications. Here are some intriguing facts about this compound:

  • Structural Complexity: The compound features a chromenone backbone, which is notable for its aromaticity and the potential for various substitutions, adding to the compound's chemical diversity.
  • Biological Activity: Compounds in the chromenone class have been studied for their various biological properties, including antibacterial, antioxidant, and anti-inflammatory activities.
  • Pharmaceutical Potential: The presence of the pyridine ring within the structure suggests that 6-nitro-3-(4-pyridyl)chromen-2-one could serve as a lead compound in drug discovery efforts, particularly in developing new therapeutics.
  • Electrophilic Nature: The nitro group in the molecule can significantly influence its electrophilic characteristics, potentially making it reactive towards nucleophiles, which is valuable in synthesizing derivatives.

Through this remarkable compound, researchers are continuing to unlock new pathways in the realm of drug design, underscoring the importance of structural optimization in enhancing biological effectiveness. As one researcher aptly stated, "Every variation opens a new door to potential discovery." This highlights the dynamic nature of small molecules like 6-nitro-3-(4-pyridyl)chromen-2-one, offering a glimpse into the possibilities of future pharmaceutical advancements.

Synonyms
3390-70-3
6-Nitro-3-(4-pyridyl)coumarin
COUMARIN, 6-NITRO-3-(4-PYRIDYL)-
BRN 0889282
DTXSID60187523
DTXCID20110014
6-Nitro-3-(pyridin-4-yl)-2H-chromen-2-one
6-nitro-3-(4-pyridinyl)-2H-chromen-2-one