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[2-(2-furyl)-1,3-dioxolan-4-yl]methanol

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Identification
Molecular formula
C7H10O3
CAS number
4469-50-7
IUPAC name
[2-(2-furyl)-1,3-dioxolan-4-yl]methanol
State
State

At room temperature, [2-(2-furyl)-1,3-dioxolan-4-yl]methanol is a liquid.

Melting point (Celsius)
-15.00
Melting point (Kelvin)
258.15
Boiling point (Celsius)
95.00
Boiling point (Kelvin)
368.00
General information
Molecular weight
142.14g/mol
Molar mass
142.1440g/mol
Density
1.2610g/cm3
Appearence

[2-(2-furyl)-1,3-dioxolan-4-yl]methanol is typically a colorless to pale yellow liquid which has a sweetish odor.

Comment on solubility

Solubility of [2-(2-furyl)-1,3-dioxolan-4-yl]methanol

[2-(2-furyl)-1,3-dioxolan-4-yl]methanol is an intriguing compound that exhibits unique solubility characteristics. Its solubility is influenced by its molecular structure, especially the presence of the furan ring and the dioxolane moiety. Here are several key points to consider regarding its solubility:

  • Polarity: The hydroxymethyl group enhances the polarity of the compound, making it more soluble in polar solvents like water.
  • Solvent Compatibility: It is likely to dissolve well in organic solvents such as ethanol or methanol due to the compatible hydrophobic furan ring.
  • Temperature Effect: The solubility of [2-(2-furyl)-1,3-dioxolan-4-yl]methanol may increase with rising temperatures, a common phenomenon in many organic compounds.
  • Hydrogen Bonding: The ability of the compound to participate in hydrogen bonding with solvents can significantly affect solubility.

As with many organic compounds, the statement that "like dissolves like" holds true here. Understanding the solubility of [2-(2-furyl)-1,3-dioxolan-4-yl]methanol is essential for its applications in pharmaceuticals and materials science. Testing in various solvents will provide a clearer picture of its solubility behavior.

Interesting facts

Interesting Facts about [2-(2-furyl)-1,3-dioxolan-4-yl]methanol

[2-(2-furyl)-1,3-dioxolan-4-yl]methanol is a fascinating compound that merges organic chemistry with the unique properties of furan derivatives. This compound features a dioxolane ring structure, which is an important motif in several natural products and synthetic molecules.

Noteworthy Attributes:

  • Furan Derivative: The presence of the furan moiety contributes to a range of reactivity and biological activity, making this compound a point of interest for chemists studying metabolic pathways and pharmacology.
  • Dioxolane Ring: The dioxolane ring enhances stability and offers a unique electronic environment, making it an excellent candidate for further functionalization and complex synthesis.
  • Potential Applications: Researchers are exploring its use in drug development, agrochemicals, and material science due to its interesting structural characteristics.
  • Versatile Intermediary: It can serve as an intermediary in organic synthesis, facilitating the construction of more complex molecular architectures.

As chemists delve deeper into the characteristics and potential applications of [2-(2-furyl)-1,3-dioxolan-4-yl]methanol, its role in biochemistry and material science continues to expand. "Innovation often arises from understanding the simplest of structures," as noted by many researchers in the field.

This compound exemplifies how a seemingly straightforward molecule can open doors to a myriad of scientific inquiries and practical applications. Through ongoing research, the exploration of [2-(2-furyl)-1,3-dioxolan-4-yl]methanol may uncover novel benefits and functionalities that are yet to be discovered.

Synonyms
1708-42-5
[2-(furan-2-yl)-1,3-dioxolan-4-yl]methanol
1,3-DIOXOLANE-4-METHANOL, 2-(alpha-FURYL)-
2-Furaldehyde, cyclic (hydroxymethyl)ethylene acetal
2-(2-Furanyl)-1,3-dioxolane-4-methanol
(2-(Furan-2-yl)-1,3-dioxolan-4-yl)methanol
NSC 26597
1,3-Dioxolane-4-methanol, 2-(2-furyl)-
2-(alpha-Furyl)-1,3-dioxolane-4-methanol
1,3-Dioxolane-4-methanol, 2-(2-furanyl)-
NSC26597
1, 2-(2-furanyl)-
1, 2-(2-furyl)-
1, 2-(.alpha.-furyl)-
SCHEMBL10000234
DTXSID90937836
NSC-26597
WLN: T5O COTJ D1Q B- BT5OJ
4-hydroxymethyl-2-(2-furyl)-1,3-dioxolane