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Methyl 3-acetyl-2-oxo-2H-chromene-6-carboxylate

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Identification
Molecular formula
C13H10O5
CAS number
23883-91-6
IUPAC name
methyl 3-acetyl-2-oxo-chromene-6-carboxylate
State
State

At room temperature, methyl 3-acetyl-2-oxo-2H-chromene-6-carboxylate exists as a solid primarily due to its crystalline nature.

Melting point (Celsius)
95.00
Melting point (Kelvin)
368.20
Boiling point (Celsius)
513.20
Boiling point (Kelvin)
786.20
General information
Molecular weight
260.23g/mol
Molar mass
260.2330g/mol
Density
1.3350g/cm3
Appearence

Methyl 3-acetyl-2-oxo-2H-chromene-6-carboxylate is typically a crystalline powder. The color of the compound can range from off-white to pale yellow, indicating its pure state.

Comment on solubility

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

Methyl 3-acetyl-2-oxo-chromene-6-carboxylate, a complex organic compound, exhibits intriguing solubility characteristics that are important for its applications in various fields.

The solubility of this compound can generally be influenced by several factors:

  • Polarity: The presence of polar functional groups, particularly the carboxylate and acetyl moieties, tends to enhance its solubility in polar solvents.
  • Solvent type: This compound is likely to be soluble in alcohols, dimethyl sulfoxide (DMSO), and acetone, while showing reduced solubility in non-polar solvents such as hexane or benzene.
  • Temperature: An increase in temperature typically leads to increased solubility for most organic compounds, including methyl 3-acetyl-2-oxo-chromene-6-carboxylate.

Therefore, it can be summarized that:

  • The compound is soluble in polar solvents.
  • It displays limited solubility in non-polar environments.

As such, understanding the solubility aspects of methyl 3-acetyl-2-oxo-chromene-6-carboxylate is crucial for its effective utilization in practical applications.

Interesting facts

Interesting Facts about Methyl 3-acetyl-2-oxo-chromene-6-carboxylate

Methyl 3-acetyl-2-oxo-chromene-6-carboxylate is a fascinating organic compound that belongs to the chromene family. This group of compounds is renowned for its diverse range of applications, particularly in the fields of pharmaceuticals and materials science. Below are some captivating aspects of this compound:

  • Diverse Biological Activity: Compounds in the chromene family, including this one, often exhibit a variety of biological activities. Methyl 3-acetyl-2-oxo-chromene-6-carboxylate has been studied for its potential as:
    • Antioxidant
    • Antimicrobial
    • Anti-inflammatory agent
  • Synthetic Versatility: This chemical structure is revered for its synthetic versatility. Chemists can use it as:
    • A building block for more complex molecules
    • A precursor in the synthesis of natural products
  • Role in Organic Chemistry: The chromene structure plays a significant role in eco-friendly organic synthesis, allowing for the development of compounds that are safer for the environment.
  • Natural Occurrence: Many chromenes are found in nature as derived compounds from plants. Their presence in natural substances often contributes to their fragrance and color.
  • Potential for Drug Development: With ongoing research into methyl 3-acetyl-2-oxo-chromene-6-carboxylate, scientists are exploring its potential as a lead compound for new drug discoveries.

As an intriguing member of the chromene family, methyl 3-acetyl-2-oxo-chromene-6-carboxylate continues to be a subject of interest within various scientific disciplines. The exploration of its properties and applications unravels numerous possibilities for innovation and advancement in both chemistry and biotechnology.

Synonyms
6468-74-2
3-Acetyl-6-carbomethoxycoumarin
BRN 1383306
SC-359
2H-1-BENZOPYRAN-6-CARBOXYLIC ACID, 3-ACETYL-2-OXO-, METHYL ESTER
3-Acetyl-2-oxo-2H-1-benzopyran-6-carboxylic acid methyl ester
DTXSID70214975
DTXCID00137466
5-18-08-00582 (beilstein handbook reference)
Methyl 3-acetyl-2-oxo-2H-chromene-6-carboxylate