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5-Methoxy-3,4-dihydroxyacetophenone

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Identification
Molecular formula
C9H10O4
CAS number
552-86-3
IUPAC name
1-(3,4-dihydroxy-5-methoxy-phenyl)ethanone
State
State

This compound is a solid at room temperature, typically found in a crystalline form.

Melting point (Celsius)
180.00
Melting point (Kelvin)
453.15
Boiling point (Celsius)
333.10
Boiling point (Kelvin)
606.25
General information
Molecular weight
196.18g/mol
Molar mass
196.1950g/mol
Density
1.2950g/cm3
Appearence

5-Methoxy-3,4-dihydroxyacetophenone appears as a yellowish crystalline solid.

Comment on solubility

Solubility Characteristics of 1-(3,4-dihydroxy-5-methoxy-phenyl)ethanone

The solubility of 1-(3,4-dihydroxy-5-methoxy-phenyl)ethanone, also known as a compound featuring a phenolic structure, can be influenced by several factors:

  • Polarity: Due to its hydroxyl (–OH) groups, this compound shows a degree of polarity which typically enhances its solubility in polar solvents, such as water.
  • Hydrogen Bonding: The presence of multiple hydroxyl groups facilitates hydrogen bonding with solvent molecules, increasing the chances of dissolution.
  • Solvent Interaction: This compound is likely more soluble in organic solvents like ethanol or methanol compared to non-polar solvents, owing to the hydrophobic methoxy group.

In general, while exploring the solubility of 1-(3,4-dihydroxy-5-methoxy-phenyl)ethanone, one might consider the following points:

  1. Examine its behavior in various solvent systems to determine the most effective medium for dissolution.
  2. Assess the temperature effects, as increased temperature can enhance solubility.
  3. Evaluate the presence of ionic species in solution, as they may influence solubility through coordination or solvation dynamics.

Overall, the solubility of this compound signifies its potential applications in various chemical and biological contexts, and understanding it allows for effective utilization in relevant fields.

Interesting facts

Interesting Facts about 1-(3,4-Dihydroxy-5-methoxy-phenyl)ethanone

1-(3,4-Dihydroxy-5-methoxy-phenyl)ethanone, commonly known as a flavonoid compound, boasts a range of intriguing features that highlight its significance in both chemistry and biology. Here are some captivating points to consider:

  • Natural Origin: This compound is often derived from natural sources, particularly plants, where it contributes to the color, flavor, and antioxidant properties. The presence of hydroxyl groups enhances its reactivity and biological activity.
  • Biological Activity: Numerous studies have showcased the potential health benefits associated with flavonoids, such as anti-inflammatory, antioxidant, and even anticancer properties. This compound plays an intriguing role in the quest for natural health solutions.
  • Pharmaceutical Interest: Due to its bioactive properties, compounds like 1-(3,4-dihydroxy-5-methoxy-phenyl)ethanone are often studied for their potential therapeutic applications, including their use in developing new medications.
  • Research Versatility: The structure of this compound allows it to be a useful model for understanding various chemical reactions and mechanisms, which are key to research in organic chemistry and pharmacology.

As science continually unveils the depths of nature's chemistry, 1-(3,4-dihydroxy-5-methoxy-phenyl)ethanone stands out as a **symbol of the intersection between chemistry and health**, showcasing how understanding molecular structures can lead to significant advancements in medicine and wellness.

In the words of the renowned chemist, "Chemistry is the science of matter, but it is also a way of thinking about the world around us." As an intriguing compound, it represents the beauty and complexity of nature's creations.

Synonyms
3934-89-2
1-(3,4-dihydroxy-5-methoxyphenyl)ethanone
ACETOPHENONE, 3,4-DIHYDROXY-5-METHOXY-
1-(3,4-Dihydroxy-5-methoxyphenyl)ethan-1-one
BRN 2267510
3,4-Dihydroxy-5-methoxyacetophenone
SCHEMBL2338863
DTXSID90192564
EN300-1829987