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Piperonal acetone

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Identification
Molecular formula
C10H10O3
CAS number
2460-69-3
IUPAC name
4-(1,3-benzodioxol-5-yl)but-3-en-2-one
State
State

Piperonal acetone is typically found in a solid crystalline form at room temperature. Its pleasant aroma is often noted even in the solid state.

Melting point (Celsius)
59.00
Melting point (Kelvin)
332.15
Boiling point (Celsius)
314.70
Boiling point (Kelvin)
587.85
General information
Molecular weight
178.19g/mol
Molar mass
176.1890g/mol
Density
1.2870g/cm3
Appearence

Piperonal acetone is a yellow crystalline solid. It is primarily recognized for its pleasant smell and is often found as part of essential oil compositions.

Comment on solubility

Solubility of 4-(1,3-benzodioxol-5-yl)but-3-en-2-one

The solubility of 4-(1,3-benzodioxol-5-yl)but-3-en-2-one, a complex organic compound, is influenced by several factors:

  • Polarity: The presence of the benzodioxole structure affects its polarity, making it somewhat hydrophobic.
  • Solvent Interaction: It tends to be more soluble in organic solvents such as ethanol, acetone, and dichloromethane compared to polar solvents like water.
  • Functional Groups: The enone functional group can participate in hydrogen bonding, potentially enhancing solubility in certain polar solvents, but the overall structure may limit this.

Solubility can vary widely. As a rule of thumb:

  • Nonpolar solvents: Increased solubility
  • Polar solvents: Limited solubility

In studies, solubility is often determined experimentally, so it is recommended to test in desired solvents to assess practical solubility conditions for various applications.

Interesting facts

Interesting Facts about 4-(1,3-benzodioxol-5-yl)but-3-en-2-one

4-(1,3-benzodioxol-5-yl)but-3-en-2-one, often referred to in the realm of organic chemistry as a derivative of coumarin<\/em>, showcases a fascinating combination of structural characteristics that contribute to its unique properties and potential applications. Here are some interesting insights:

  • Natural Occurrence: This compound is found in various plants and may play a role in their defense mechanisms against herbivores and pathogens.
  • Synthetic Applications: The structure of this compound allows it to serve as a precursor in the synthesis of more complex organic molecules, making it valuable in pharmaceutical chemistry.
  • Biological Activity: Research has indicated that compounds related to this structure possess significant biological activities, including antioxidant<\/em>, anti-inflammatory<\/em>, and possible anticancer<\/em> properties.
  • Fluorescent Properties: Certain derivatives exhibit fluorescence, which can be harnessed for biochemical assays and imaging techniques.

One of the most intriguing aspects of 4-(1,3-benzodioxol-5-yl)but-3-en-2-one is its versatility in organic synthesis. As stated by prominent chemists: "The beauty of organic compounds lies in their ability to transform and lead to innovations in drug development."
The ongoing research into this compound may pave the way for future advancements in medicinal chemistry, and understanding its structure-activity relationship is crucial for unlocking its full potential.

Synonyms
DTXSID7025926
Piperonylidenaceton
22214-31-9
4-(1,3-dioxaindan-5-yl)but-3-en-2-one
(E)-4-(1,3-benzodioxol-5-yl)-3-buten-2-one
SCHEMBL2027162
CHEMBL3185066
DB-048076
NS00029151
1-(3,4-methylenedioxyphenyl)but-1-en-3-one
1-(3,4-methylenedioxyphenyl)-but-1-en-3-one