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2H-Chromene-3-carboxamide

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Identification
Molecular formula
C10H9NO2
CAS number
193611-85-9
IUPAC name
2H-chromene-3-carboxamide
State
State

At room temperature, 2H-Chromene-3-carboxamide is generally a solid. It is stable under normal conditions but should be handled in a well-ventilated area to avoid inhalation of any dust particles.

Melting point (Celsius)
184.00
Melting point (Kelvin)
457.00
Boiling point (Celsius)
356.00
Boiling point (Kelvin)
629.00
General information
Molecular weight
175.18g/mol
Molar mass
175.1840g/mol
Density
1.1500g/cm3
Appearence

2H-Chromene-3-carboxamide appears as a pale yellow crystalline solid. It is typically available in powder form and may vary slightly in shade based on the level of purity and method of preparation.

Comment on solubility

Solubility of 2H-chromene-3-carboxamide (C10H9NO2)

2H-chromene-3-carboxamide is an intriguing compound when it comes to solubility. Its behavior in different solvents can shed light on its potential applications in various fields.

Key Points About Solubility:

  • Polar Solvents: 2H-chromene-3-carboxamide is likely to exhibit better solubility in polar solvents due to the presence of the carboxamide functional group.
  • Non-Polar Solvents: Conversely, it may have limited solubility in non-polar solvents, which is characteristic of many compounds that contain functional groups with polar characteristics.
  • Hydrogen Bonding: The ability of this compound to engage in hydrogen bonding can enhance its solubility in aqueous solutions.
  • Applications in Pharmaceuticals: Due to its potentially favorable solubility profile, this compound could be advantageous in drug formulation, particularly in enhancing bioavailability.

In summary, the solubility of 2H-chromene-3-carboxamide can be attributed to its molecular structure and functional groups, making it a compound of interest in both the chemical and pharmaceutical industries. As one might say, "solubility is not just a property, but a key to unlocking the potential of a compound."

Interesting facts

Interesting Facts about 2H-chromene-3-carboxamide

2H-chromene-3-carboxamide is an intriguing compound that belongs to the family of chromenes, which are known for their diverse biological activities and applications in various fields. Here are some captivating insights about this compound:

  • Antioxidant Properties: Compounds in the chromene family often exhibit strong antioxidant activity, which can help combat oxidative stress in biological systems, potentially leading to health benefits.
  • Biological Significance: Research indicates that derivatives of 2H-chromene-3-carboxamide show promise in medicinal chemistry, particularly in the development of anti-inflammatory and anticancer agents.
  • Flavonoid Connection: Chromenes are structurally related to flavonoids, a group of compounds known for their role in plant coloration and their numerous health benefits. This connection highlights the potential of 2H-chromene-3-carboxamide in pharmacological studies.
  • Versatile Synthesis: The synthesis of 2H-chromene-3-carboxamide can often be achieved through several methods, making it a versatile compound for organic chemists. Techniques can include classical condensation reactions and modern methodologies like microwave-assisted synthesis.
  • Environmental Applications: There is a burgeoning interest in the application of chromene derivatives, including 2H-chromene-3-carboxamide, in environmental chemistry, particularly in the development of biodegradable materials and green solvents.

In summary, 2H-chromene-3-carboxamide is not just a generic chemical; it embodies a rich history of research and inspiration for future innovations. As quoted in scientific literature, "the exploration of chromene derivatives continues to unlock new avenues in both chemistry and biology.”

Synonyms
Compound 69/20
Compound 69-20
2H-1-BENZOPYRAN-3-CARBOXAMIDE
delta(sup 3)-Chromene-3-carboxamide
BRN 1369323
delta(3)-chromene-3-carboxamide
DTXSID80144274
5-18-06-00445 (Beilstein Handbook Reference)
DTXCID8066765
2H-chromene-3-carboxamide
10185-00-9
2H-Chromene-3-carboxylic acid amide
MFCD01662338
chromene-3-carboxamide
SCHEMBL545827
AKOS006243272
CS-0306447
AB00996836-01
Z145120524
WRJ