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(2,5-dimethyl-1H-pyrrol-3-yl)-(2-furyl)methanone

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Identification
Molecular formula
C12H13NO2
CAS number
82048-17-3
IUPAC name
(2,5-dimethyl-1H-pyrrol-3-yl)-(2-furyl)methanone
State
State

At room temperature, (2,5-dimethyl-1H-pyrrol-3-yl)-(2-furyl)methanone is typically found in the solid state.

Melting point (Celsius)
109.00
Melting point (Kelvin)
382.15
Boiling point (Celsius)
344.00
Boiling point (Kelvin)
617.15
General information
Molecular weight
187.24g/mol
Molar mass
187.2210g/mol
Density
1.1647g/cm3
Appearence

(2,5-Dimethyl-1H-pyrrol-3-yl)-(2-furyl)methanone generally appears as a light yellow crystalline solid.

Comment on solubility

Solubility Considerations for (2,5-dimethyl-1H-pyrrol-3-yl)-(2-furyl)methanone

The solubility of (2,5-dimethyl-1H-pyrrol-3-yl)-(2-furyl)methanone can be quite intriguing due to its unique chemical structure. Understanding its solubility is crucial for applications in organic chemistry and pharmaceuticals.

Factors Affecting Solubility

Several factors influence the solubility of this compound:

  • Polarity: The presence of polar functional groups may enhance solubility in polar solvents, while non-polar regions may favor solubility in non-polar solvents.
  • Hydrogen Bonding: Any ability to form hydrogen bonds can significantly increase solubility, especially in protic solvents such as water.
  • Molecular Size: Larger molecular size can hinder solubility due to steric hindrance, affecting how the compound interacts with solvents.

Typical Solvent Behavior

This compound is likely to exhibit moderate solubility in organic solvents like:

  • Acetone
  • Ethyl acetate
  • Methanol

However, it may show limited solubility in water and other highly polar solvents due to its overall structural compatibility.

Practical Implications

When conducting experiments or formulating products with (2,5-dimethyl-1H-pyrrol-3-yl)-(2-furyl)methanone, consider the following:

  • Choosing the right solvent is essential for maximizing solubility and ensuring effective reactions.
  • Pay attention to temperature, as it can significantly alter solubility characteristics of this compound.

In conclusion, the solubility of (2,5-dimethyl-1H-pyrrol-3-yl)-(2-furyl)methanone is determined by a complex interplay of structural features and environmental conditions. As with many organic compounds, understanding these nuances can aid in the effective utilization of this compound in various chemical applications.

Interesting facts

Interesting Facts about (2,5-Dimethyl-1H-pyrrol-3-yl)-(2-furyl)methanone

(2,5-Dimethyl-1H-pyrrol-3-yl)-(2-furyl)methanone is a fascinating compound that belongs to the realm of organic chemistry, specifically within the family of pyrroles and furans, which are known for their diverse applications in various fields.

Chemical Family and Structure

This compound showcases the interesting fusion of two distinct aromatic systems: the pyrrole and the furan. Pyrrole is a five-membered heterocyclic compound containing nitrogen, while furan is a five-membered ring containing oxygen. Such combinations often lead to:

  • Enhanced reactivity
  • Unique electronic properties
  • Potential for biological activity

Biological Significance

Compounds featuring both pyrrole and furan moieties have been extensively studied for their biological implications:

  • They exhibit pharmacological properties, including anti-cancer, anti-inflammatory, and antimicrobial activities.
  • Many naturally occurring compounds contain similar structures, which suggests potential medicinal uses.

Applications

The intriguing characteristics of (2,5-dimethyl-1H-pyrrol-3-yl)-(2-furyl)methanone highlight its potential in:

  • Organic synthesis as a building block for more complex molecules.
  • Specialty chemicals used in dyes, pigments, or releases.
  • Investigations into the behavior of heterocyclic compounds under various conditions.

Conclusion

As scientists continue to explore compounds like (2,5-dimethyl-1H-pyrrol-3-yl)-(2-furyl)methanone, we find ourselves unlocking a treasure trove of knowledge that bridges the gap between chemical structure and functional application. It is a prime example of how small changes in molecular architecture can lead to significant alterations in properties and functions, showcasing the beauty and complexity of organic chemistry.

Synonyms
2,5-Dimethylpyrrol-3-yl-2-furylketone
23257-55-8
UNII-2832GUY27W
2832GUY27W
DTXSID70177834
Methanone, (2,5-dimethyl-1H-pyrrol-3-yl)-2-furanyl-
KETONE, 2,5-DIMETHYLPYRROL-3-YL 2-FURYL
RefChem:82974
DTXCID30100325
Q27254255