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Coumachlor

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Identification
Molecular formula
C25H25NO3
CAS number
140-57-8
IUPAC name
7-[2-(diethylamino)ethoxy]-3,4-diphenyl-chromen-2-one
State
State

At room temperature, coumachlor is usually in a solid state.

Melting point (Celsius)
162.30
Melting point (Kelvin)
435.45
Boiling point (Celsius)
525.40
Boiling point (Kelvin)
798.55
General information
Molecular weight
365.48g/mol
Molar mass
365.4510g/mol
Density
1.2305g/cm3
Appearence

Coumachlor typically appears as a solid and may exhibit a crystalline form. It is often white or off-white in color.

Comment on solubility

Solubility of 7-[2-(diethylamino)ethoxy]-3,4-diphenyl-chromen-2-one

The solubility of 7-[2-(diethylamino)ethoxy]-3,4-diphenyl-chromen-2-one can be quite complex and may vary depending on several factors. Here are some key points to consider:

  • Solvent Dependence: This compound's solubility may be significantly influenced by the choice of solvent. In general, compounds with a large aromatic structure often show higher solubility in organic solvents.
  • Polarity: Since diethylamino groups enhance the polarity of the molecule, the compound may demonstrate increased solubility in polar solvents compared to nonpolar ones.
  • Temperature Influence: Solubility often increases with temperature. Therefore, evaluating the solubility of this compound at various temperatures could provide valuable insights.
  • pH Sensitivity: The presence of an amine group may contribute to the compound's solubility behavior in different pH environments, particularly in aqueous solutions.

Overall, understanding the solubility of this compound requires careful consideration of its structural characteristics and environmental conditions. As a guiding principle, always remember: "Like dissolves like." Exploring its solubility across different media is essential for applications in medicinal chemistry, material sciences, and chemical formulations.

Interesting facts

Interesting Facts About 7-[2-(diethylamino)ethoxy]-3,4-diphenyl-chromen-2-one

The compound 7-[2-(diethylamino)ethoxy]-3,4-diphenyl-chromen-2-one belongs to a class of molecules known as flavonoids, which are renowned for their diverse biological activities. This specific compound is particularly interesting due to its unique structure and potential applications in various fields.

Potential Applications

  • Pharmaceutical Industry: Researchers are investigating the flavonoid's properties for potential use in medicinal chemistry, particularly for its antioxidant and anti-inflammatory effects.
  • Agricultural Uses: Its ability to interact with specific biological pathways may lead to applications in developing natural pesticides or growth enhancers.
  • Cosmetic Formulations: The compound's antioxidant properties make it a candidate for use in skincare products aimed at reducing the signs of aging and protecting skin from UV damage.

Structural Significance

The structure of 7-[2-(diethylamino)ethoxy]-3,4-diphenyl-chromen-2-one features a chromenone backbone, which is crucial for its biological activity. This configuration allows the molecule to engage in:

  • Hydrogen Bonding: Enhancing its ability to interact with biological targets, possibly leading to therapeutic effects.
  • Electron Delocalization: Which contributes to stability and can influence the molecule's reactivity in biological systems.

Future Research Directions

Imagine the possibilities! As scientists continue to explore the full potential of this compound, several research questions arise:

  • What are its specific mechanisms of action in biological systems?
  • Can modifications to its structure enhance its efficacy as a pharmaceutical agent?
  • What is its interaction profile with enzymes and receptors?

As we delve deeper into the world of flavonoid compounds such as 7-[2-(diethylamino)ethoxy]-3,4-diphenyl-chromen-2-one, we uncover not only their scientific value but also their potential to significantly impact health, agriculture, and cosmetics. In the words of many chemists, "Each compound tells a story," and this one is just beginning to unfold.

Synonyms
1762-91-0
COUMARIN, 7-(2-(DIETHYLAMINO)ETHOXY)-3,4-DIPHENYL-
7-(2-(Diethylamino)ethoxy)-3,4-diphenylcoumarin
7-(2-(Diethylamino)ethoxy)-3,4-diphenyl-2H-chromen-2-one
7-[2-(diethylamino)ethoxy]-3,4-diphenyl-2H-chromen-2-one
BRN 1297147
7-[2-(Diethylamino)ethoxy]-3,4-diphenylcoumarin
Coumarin, 7-[2-(diethylamino)ethoxy]-3,4-diphenyl-
AC2GM7W4DA
DTXSID40170099
7-[2-(Diethylamino)ethoxy]-3,4-diphenyl-2H-1-benzopyran-2-one
2H-1-Benzopyran-2-one, 7-[2-(diethylamino)ethoxy]-3,4-diphenyl-