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6-Amino-3-(morpholine-4-carbonyl)chromen-2-one

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Identification
Molecular formula
C14H14N2O4
CAS number
676127-83-6
IUPAC name
6-amino-3-(morpholine-4-carbonyl)chromen-2-one
State
State

At room temperature, this compound is a solid.

Melting point (Celsius)
250.00
Melting point (Kelvin)
523.15
Boiling point (Celsius)
510.00
Boiling point (Kelvin)
783.15
General information
Molecular weight
260.27g/mol
Molar mass
260.2700g/mol
Density
1.3000g/cm3
Appearence

This compound appears as a crystalline solid, typically in an off-white to pale yellow color. The crystalline structure is typical for many organic compounds, featuring a solid and stable form at room temperature.

Comment on solubility

Solubility of 6-amino-3-(morpholine-4-carbonyl)chromen-2-one

The solubility of 6-amino-3-(morpholine-4-carbonyl)chromen-2-one can be complex due to its unique structure. Some aspects to consider include:

  • Polarity: The presence of amino and carbonyl groups can make the molecule polar, potentially enhancing its solubility in polar solvents.
  • Solvent Interaction: It is likely to be more soluble in solvents such as water and methanol, which can stabilize the polar functional groups.
  • pH Dependence: The solubility may also vary with pH; as the amino group can be protonated under acidic conditions, affecting solubility.
  • Hydrogen Bonding: The ability to form hydrogen bonds with solvents could further enhance solubility, particularly in protic solvents.

In summary, 6-amino-3-(morpholine-4-carbonyl)chromen-2-one is expected to exhibit variable solubility depending on the solvent and conditions employed. An understanding of these factors is crucial for its application in various fields.

Interesting facts

Interesting Facts about 6-amino-3-(morpholine-4-carbonyl)chromen-2-one

6-amino-3-(morpholine-4-carbonyl)chromen-2-one is a fascinating compound with a variety of applications and implications in the field of chemistry and medicinal sciences. Here are some intriguing points to consider:

  • Structural Complexity: This compound belongs to the class of chromenones, which are known for their unique bicyclic structure. The presence of the morpholine moiety adds to its complexity, giving it unique properties.
  • Pharmaceutical Potential: Compounds like 6-amino-3-(morpholine-4-carbonyl)chromen-2-one have been studied for their biological activities. They may exhibit anti-inflammatory, antimicrobial, and even anticancer properties.
  • Versatility in Synthesis: The synthetic pathways leading to this compound can vary widely, allowing chemists to explore different reaction conditions and modifications to tailor its properties for specific applications.
  • Research Interest: As researchers continue to investigate the potential of chromenones in drug discovery, compounds such as this one are at the forefront, providing insight into how small changes in structure can lead to significant changes in biological activity.
  • Academic Focus: In the realm of academic research, exploring derivatives of chromenones can enrich our understanding of reaction mechanisms, molecular interactions, and the importance of functional groups in determining the overall behavior of compounds.

In summary, the compound 6-amino-3-(morpholine-4-carbonyl)chromen-2-one serves as a perfect example of how a complex organic molecule can bridge the gap between chemical structure and biological function. Its ongoing study could uncover new horizons in medicinal chemistry!

Synonyms
18144-57-5
6-Amino-3-(morpholinocarbonyl)coumarin
BRN 1149929
COUMARIN, 6-AMINO-3-(MORPHOLINOCARBONYL)-
DTXSID50171153
DTXCID9093644
6-amino-3-(morpholine-4-carbonyl)chromen-2-one
6-Amino-3-(morpholine-4-carbonyl)-2H-chromen-2-one