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Furoin

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Identification
Molecular formula
C13H10O2
CAS number
552-86-3
IUPAC name
3-(2-furyl)-1-phenyl-prop-2-en-1-one
State
State

At room temperature, furoin is in a crystalline solid state. It is stable under standard conditions and does not readily vaporize.

Melting point (Celsius)
84.00
Melting point (Kelvin)
357.15
Boiling point (Celsius)
356.00
Boiling point (Kelvin)
629.15
General information
Molecular weight
198.22g/mol
Molar mass
198.2100g/mol
Density
1.2170g/cm3
Appearence

Furoin typically appears as an off-white to pale yellow crystalline solid. It has a distinct aromatic odor and is known for its crystalline texture.

Comment on solubility

Solubility of 3-(2-furyl)-1-phenyl-prop-2-en-1-one

The compound 3-(2-furyl)-1-phenyl-prop-2-en-1-one is known for its intriguing solubility characteristics. In the context of organic compounds, solubility is a significant factor for practical applications and can often dictate its behavior in various environments. Here are some key points regarding its solubility:

  • Polarity: The presence of the furan ring in the structure introduces a certain polarity, which affects how the compound interacts with solvents.
  • Solvent Compatibility: This compound is generally more soluble in polar organic solvents such as ethanol or acetone, as opposed to nonpolar solvents.
  • Temperature Dependence: Like many organic compounds, its solubility may increase with temperature, enabling better dissolution.
  • Impurities: The presence of impurities can also play a role in solubility dynamics, potentially enhancing or hindering dissolution in specific solvents.

As a rule of thumb, “like dissolves like” frequently holds true, meaning that polar compounds tend to be soluble in polar solvents. Therefore, understanding the solubility behavior of 3-(2-furyl)-1-phenyl-prop-2-en-1-one can be pivotal for its application in fields like pharmaceuticals, agrochemicals, and material science.

Interesting facts

Interesting Facts about 3-(2-furyl)-1-phenyl-prop-2-en-1-one

3-(2-furyl)-1-phenyl-prop-2-en-1-one, commonly referred to as a type of chalcone, is a fascinating compound known for its unique structural and chemical properties. This compound can be explored from various scientific angles:

  • Versatile Precursor: Chalcones, such as 3-(2-furyl)-1-phenyl-prop-2-en-1-one, serve as versatile intermediates in the synthesis of a wide array of bioactive compounds. Due to their endowment of a reactive α,β-unsaturated carbonyl system, they can readily participate in several chemical reactions.
  • Biological Activity: Many chalcones exhibit significant biological activities. Research has indicated that compounds like 3-(2-furyl)-1-phenyl-prop-2-en-1-one may possess anti-inflammatory, antifungal, and anticancer properties, making them subjects of interest within medicinal chemistry.
  • Aromatic Character: The presence of both furan and phenyl groups gives 3-(2-furyl)-1-phenyl-prop-2-en-1-one a distinct aromatic character. Aromatic compounds are known for their stability and unique reactivity due to their π-electron systems.
  • Applications in Organic Synthesis: This compound is often utilized in organic synthesis and may serve as a building block for more complex molecules, demonstrating significant utility in designing new pharmaceuticals.
  • Natural Occurrence: Chalcones are found in various plants, and the study of 3-(2-furyl)-1-phenyl-prop-2-en-1-one can lead to insights into the biosynthetic pathways of natural products.

In summary, 3-(2-furyl)-1-phenyl-prop-2-en-1-one is not only interesting due to its chemical structure but also its potential as a bioactive compound and a precursor in synthetic organic chemistry. As a scientist or a chemistry student, delving into the properties and applications of this compound opens up a world of possibilities in research and development.

Synonyms
DTXSID00870760
SB61123