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Ethyl 3-acetyl-2-oxo-chromene-6-carboxylate

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Identification
Molecular formula
C14H12O5
CAS number
3333-23-7
IUPAC name
ethyl 3-acetyl-2-oxo-chromene-6-carboxylate
State
State

At room temperature, Ethyl 3-acetyl-2-oxo-chromene-6-carboxylate is in a solid state. The compound remains stable under standard conditions, making it easy to handle and store.

Melting point (Celsius)
87.00
Melting point (Kelvin)
360.15
Boiling point (Celsius)
400.00
Boiling point (Kelvin)
673.15
General information
Molecular weight
275.26g/mol
Molar mass
275.2610g/mol
Density
1.2970g/cm3
Appearence

Ethyl 3-acetyl-2-oxo-chromene-6-carboxylate appears as a pale yellow to off-white crystalline powder. Its solid form is typically characterized by a fine crystalline structure that makes it distinct under visual inspection.

Comment on solubility

Solubility of Ethyl 3-Acetyl-2-Oxo-Chromene-6-Carboxylate

Ethyl 3-acetyl-2-oxo-chromene-6-carboxylate is a fascinating compound recognized for its unique solubility characteristics. Its solubility can be influenced by various factors, making it essential to consider specific solvents for effective application:

  • Polar Solvents: This compound exhibits good solubility in polar solvents such as ethanol and methanol. The presence of polar functional groups enhances its interaction with these solvents.
  • Apolar Solvents: Conversely, ethyl 3-acetyl-2-oxo-chromene-6-carboxylate shows limited solubility in non-polar solvents like hexane or chloroform, demonstrating its hydrophilic tendencies.
  • Temperature Dependence: The solubility of this compound can vary with temperature. Generally, increasing the temperature improves solubility in polar solvents.

It is often noted that solubility plays a crucial role in the chemical applications of this compound, with quotes like “The solution to solubility lies in the solvent choice” being particularly relevant. Understanding these solubility attributes enables chemists to effectively manipulate conditions for desired reactions.

As you explore its applications, keep in mind the solvent interactions that govern its behavior!

Interesting facts

Interesting Facts About Ethyl 3-acetyl-2-oxo-chromene-6-carboxylate

Ethyl 3-acetyl-2-oxo-chromene-6-carboxylate is a fascinating compound that showcases the intricate world of organic chemistry. This compound belongs to the chromene family, which are derivatives of chromen-4-one, a naturally occurring structure that plays significant roles in various biological processes.

Key Characteristics

  • Biological Activity: Compounds like ethyl 3-acetyl-2-oxo-chromene-6-carboxylate often exhibit remarkable biological activities, including antioxidant, anti-inflammatory, and even anticancer properties, making them subjects of intense research.
  • Synthetic Utility: This compound serves as a precursor in the synthesis of more complex organic molecules. Its versatile structure enables it to participate in multiple reactions, thus expanding its applicability in various fields.
  • Research Interest: The study of chromenes is significant in medicinal chemistry, as scientists explore their potential in drug development due to their diverse pharmacological profiles.

Quote from Chemistry Insight

"Every compound tells a story—unfolding layers of reactivity, biological significance, and potential applications." This statement resonates profoundly within the context of ethyl 3-acetyl-2-oxo-chromene-6-carboxylate, inviting both scientists and students alike to delve deeper into its wonders.

In summary, ethyl 3-acetyl-2-oxo-chromene-6-carboxylate not only highlights the complexity of organic molecules but also paves the way for innovative research in chemistry and beyond. Its potential applications and biological significance are truly what make chemistry an exciting field to explore!

Synonyms
6468-75-3
3-Acetyl-6-carbethoxycoumarin
BRN 1386325
SC-360
2H-1-BENZOPYRAN-6-CARBOXYLIC ACID, 3-ACETYL-2-OXO-, ETHYL ESTER
3-Acetyl-2-oxo-2H-1-benzopyran-6-carboxylic acid ethyl ester
DTXSID30214976
DTXCID60137467
5-18-08-00582 (beilstein handbook reference)
ethyl 3-acetyl-2-oxo-2H-chromene-6-carboxylate