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Nitrocoumarin

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Identification
Molecular formula
C14H8N2O4
CAS number
2439-72-3
IUPAC name
6-nitro-3-(2-pyridyl)chromen-2-one
State
State

At room temperature, Nitrocoumarin is a crystalline solid. The compound is stable under standard conditions and is typically stored in a cool, dry place to maintain its integrity.

Melting point (Celsius)
148.00
Melting point (Kelvin)
421.15
Boiling point (Celsius)
180.00
Boiling point (Kelvin)
453.15
General information
Molecular weight
272.22g/mol
Molar mass
272.2160g/mol
Density
1.3961g/cm3
Appearence

Nitrocoumarin typically appears as a yellow crystalline solid. The vibrant yellow hue is characteristic of many nitroaromatic compounds, offering it a distinct appearance.

Comment on solubility

Solubility of 6-Nitro-3-(2-pyridyl)chromen-2-one

The solubility of 6-nitro-3-(2-pyridyl)chromen-2-one, a compound known for its intriguing chemical structure, can be assessed through several important factors:

  • Polarity: This compound features both polar and non-polar functional groups, which can influence its overall solubility in different solvents.
  • Solvent Interaction: Typically, compounds like this may dissolve well in organic solvents such as dimethyl sulfoxide (DMSO) and ethanol, while showing limited solubility in water due to hydrophobic interactions.
  • Influence of Substituents: The presence of the nitro group, a significant electron-withdrawing group, can affect the distribution of electron density and subsequently the solubility profile.
  • Temperature Dependency: As with many organic compounds, solubility increases with temperature. Hence, heating the solvent can often enhance solubility.

In conclusion, while 6-nitro-3-(2-pyridyl)chromen-2-one demonstrates moderate solubility in organic solvents, its solubility in aqueous environments is notably low. As a result, understanding these factors is crucial for applications involving this compound in chemical processes.

Interesting facts

Interesting Facts about 6-nitro-3-(2-pyridyl)chromen-2-one

6-nitro-3-(2-pyridyl)chromen-2-one is a fascinating chemical compound that belongs to the family of chromenones, which are aromatic compounds known for their significant biological activities. Here are some compelling facts about this intriguing molecule:

  • Structure and Functionality: This compound features a chromenone backbone, which is linked to a nitro group and a pyridine ring. The unique structure contributes to its diverse properties and potential applications in medicinal chemistry.
  • Biological Activity: Compounds in the chromenone family have been researched for various biological activities, including anti-inflammatory, antioxidant, and antibacterial effects. 6-nitro-3-(2-pyridyl)chromen-2-one is no exception, and its derivatives can be explored for therapeutic uses.
  • Fluorescent Properties: Certain chromenones exhibit fluorescence, making them valuable in analytical applications and as fluorescent probes in biological studies. Research on the photophysical properties of this compound could yield significant insights.
  • Drug Development: The presence of both nitro and pyridyl moieties may enhance the compound's interaction with biological targets, paving the way for its use in drug development and research into new therapeutic agents.
  • Research Potential: Ongoing studies are likely to focus on exploring its applications within pharmacology and biochemistry. The exploration of novel derivatives could lead to the discovery of new compounds with improved efficacy and specificity.

Ultimately, 6-nitro-3-(2-pyridyl)chromen-2-one is not just a straightforward chemical entity; it embodies potential pathways for future scientific exploration and notable applications in various fields, including pharmaceuticals and biological research.

Synonyms
6-Nitro-3-(2-pyridyl)coumarin
3390-73-6
COUMARIN, 6-NITRO-3-(2-PYRIDYL)-
BRN 0889281
DTXSID80187525
DTXCID40110016
6-nitro-3-(pyridin-2-yl)-2H-chromen-2-one
Oprea1_055896
6-nitro-3-(2-pyridinyl)-2H-chromen-2-one
SR-01000424249
SR-01000424249-1