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2-Phenyl-1,3-dioxolan-4-ylmethanol

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Identification
Molecular formula
C10H12O3
CAS number
30334-69-1
IUPAC name
(2-phenyl-1,3-dioxolan-4-yl)methanol
State
State

At room temperature, 2-Phenyl-1,3-dioxolan-4-ylmethanol is typically found in a solid state, often as a crystalline or powder form.

Melting point (Celsius)
65.00
Melting point (Kelvin)
338.15
Boiling point (Celsius)
285.00
Boiling point (Kelvin)
558.15
General information
Molecular weight
180.20g/mol
Molar mass
180.2040g/mol
Density
1.1765g/cm3
Appearence

2-Phenyl-1,3-dioxolan-4-ylmethanol typically appears as a white to off-white crystalline powder. It may also appear in the form of a crystalline solid that is colorless.

Comment on solubility

Solubility of (2-phenyl-1,3-dioxolan-4-yl)methanol

The solubility of (2-phenyl-1,3-dioxolan-4-yl)methanol can vary significantly based on several factors. Generally, this synthetic compound exhibits a range of solubility characteristics that are important to consider:

  • Polarity: The presence of a dioxolane ring and a hydroxyl group can contribute to its polarity, enhancing solubility in polar solvents such as water.
  • Hydrogen Bonding: The hydroxyl (-OH) group can engage in hydrogen bonding, potentially increasing solubility in polar solvents.
  • Solvent Compatibility: In non-polar solvents, its solubility may significantly decrease due to the hydrophobic nature of the phenyl group.
  • Concentration and Temperature: Solubility is also dependent on concentration and temperature; higher temperatures often enhance solubility.

In summary, while (2-phenyl-1,3-dioxolan-4-yl)methanol may dissolve well in polar solvents, one must consider the influence of structural characteristics and environmental conditions. As a rule of thumb, "like dissolves like"—polar substances tend to dissolve well in polar environments.

Interesting facts

Exploring (2-phenyl-1,3-dioxolan-4-yl)methanol

(2-phenyl-1,3-dioxolan-4-yl)methanol is a fascinating compound that showcases the intricate interplay between organic chemistry and functionality. This compound consists of a dioxolane ring, which imparts unique properties due to its structural characteristics. Here are some interesting facts to consider:

  • Structural Diversity: The presence of a phenyl group in its structure not only contributes to its aromatic nature but also influences reactivity and stability in various chemical reactions.
  • Potential Applications: Compounds with dioxolane rings have been investigated for their applications in medicinal chemistry, particularly in the development of pharmaceuticals and biologically active compounds.
  • Synthesis Interest: The synthesis of (2-phenyl-1,3-dioxolan-4-yl)methanol can inspire students and researchers alike to explore innovative methodologies in organic synthesis, particularly through methods like ring formation and functional group interconversions.
  • Research Opportunities: Given its unique molecular framework, this compound can serve as a starting material for a wide range of derivatives, highlighting the importance of studying such compounds to expand the horizons of organic synthesis.
  • Environmental Aspects: Compounds that contain carbon-oxygen frameworks, including dioxolanes, have garnered attention regarding their environmental impact and potential as green solvents or intermediates in sustainable chemical processes.

Overall, (2-phenyl-1,3-dioxolan-4-yl)methanol is a prime example of how organic compounds can bridge chemistry with practical applications in various fields, making it an intriguing subject of study for chemists at any level.

Synonyms
(2-phenyl-1,3-dioxolan-4-yl)methanol
1708-39-0
2-Phenyl-1,3-dioxolane-4-methanol
Benzal glyceryl acetal
Benzylidene glycerol
4-(Hydroxymethyl)-2-phenyldioxolane
Glycerol, 1,2-O-benzylidene-
Benzaldehyde, cyclic (hydroxymethyl)ethylene acetal
EINECS 216-962-1
NSC 78968
1,3-DIOXOLANE-4-METHANOL, 2-PHENYL-
BRN 0156802
4JD6JK979Y
AI3-18077
NSC-78968
DTXSID70937834
5-19-02-00562 (Beilstein Handbook Reference)
BENZALDEHYDE 1,2-GLYCERYL ACETAL
DTXCID70906020
216-962-1
1,2-Benzylideneglycerol
2-Phenyl-m-dioxan-5-ol
2-PHENYL-1.3-DIOXOLANE-4-METHANOL
4-hydroxymethyl-2-phenyl-1,3-dioxolane
UNII-4JD6JK979Y
1,2-O-Benzylideneglycerol
Glycerol,2-O-benzylidene-
NCIOpen2_000955
1,2-O-Benzylidene-Glycerol
SCHEMBL4812494
Glycerol 1,2-benzylidene ether
AUDDNHGBAJNKEH-UHFFFAOYSA-N
CHEBI:168389
WLN: T5O COTJ BR& D1Q
NSC78968
MFCD00152747
1,3-Dioxolane-4-methanol,2-phenyl-
AKOS006274417
NS00047670
Q27259748