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2-Benzyl-1,3-dioxolane

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Identification
Molecular formula
C10H12O2
CAS number
4435-48-7
IUPAC name
2-benzyl-1,3-dioxolane
State
State

At room temperature, 2-benzyl-1,3-dioxolane is a liquid.

Melting point (Celsius)
-45.00
Melting point (Kelvin)
228.15
Boiling point (Celsius)
242.00
Boiling point (Kelvin)
515.15
General information
Molecular weight
164.20g/mol
Molar mass
164.2040g/mol
Density
1.0770g/cm3
Appearence

2-Benzyl-1,3-dioxolane is a clear, colorless liquid with a pleasant aromatic odor. It is typically found in liquid form under standard conditions.

Comment on solubility

Solubility of 2-benzyl-1,3-dioxolane

2-benzyl-1,3-dioxolane, a compound with a unique structure, exhibits interesting solubility characteristics that are crucial for its application in various chemical processes. This compound is known to be soluble in organic solvents such as:

  • Diethyl ether
  • Tetrahydrofuran (THF)
  • Acetone
  • Chloroform

However, it is notably insoluble in water. This lack of solubility in polar solvents can be attributed to its non-polar benzyl group and the inherent characteristics of the dioxolane ring, which disrupt the intermolecular hydrogen bonding that is essential for solubility in water. Furthermore, it is important to recognize the implications of its solubility:

  1. Solubility in organic solvents allows for easier incorporation in synthetic reactions and applications.
  2. Insolubility in water suggests limited interactions in aqueous environments, affecting potential biological activity.
  3. Understanding its solubility profile is essential for proper storage and handling in laboratory settings.

As with many organic compounds, the solubility of 2-benzyl-1,3-dioxolane can significantly influence its reactivity and usability, making it a compelling subject of study for chemists.

Interesting facts

Interesting Facts about 2-Benzyl-1,3-Dioxolane

2-Benzyl-1,3-dioxolane is an intriguing chemical compound that stands out due to its unique structure and potential applications. As a member of dioxolane compounds, which are known for their cyclic ether characteristics, it possesses interesting properties that make it a subject of study in organic chemistry.

Key Highlights:

  • Structural Components: The compound features a benzyl group attached to a dioxolane ring, which enhances its stability and aromatic properties.
  • Reactivity: The presence of the dioxolane structure often allows for *nucleophilic attack*, making it useful in various organic synthesis reactions.
  • Applications: Researchers have explored the use of 2-benzyl-1,3-dioxolane in fields such as:
    • Pharmaceuticals: Potentially as an intermediate in the synthesis of biologically active compounds.
    • Material Science: Used in the development of new materials with specific functional properties.
  • Synthetic Utility: Its unique structure allows it to serve as a *protecting group* in organic synthesis, often resulting in more efficient synthetic routes.

In summary, 2-benzyl-1,3-dioxolane is not just another compound; it embodies the convergence of structural elegance and practical application. As we continue to delve into the *intricacies of organic compounds*, understanding the unique aspects of compounds like 2-benzyl-1,3-dioxolane can open new avenues for innovation in both academic and industrial chemistry.

Synonyms
2-Benzyl-1,3-dioxolane
101-49-5
1,3-Dioxolane, 2-(phenylmethyl)-
2-Benzyldioxolan
Phenylacetaldehyde ethylene acetal
Phenylacetaldehyde glycol acetal
1,3-DIOXOLANE, 2-BENZYL-
Phenylacetaldehyde ethyleneglycol acetal
NSC-25480
1,3-Dioxolane,2-(phenylmethyl)-
EINECS 202-946-1
NSC 25480
benzyldioxolan
BRN 0117974
Phenylacetaldehyde ethylene glycol acetal
AI3-31161
MFCD00003215
1, 2-benzyl-
2-Benzyl-[1,3]dioxolane
SCHEMBL22722
WLN: T5O COTJ B1R
2-phenylmethyl 1,3-dioxolane
DTXSID1059230
SSZACLYPEFCREM-UHFFFAOYSA-
2-(phenylmethyl)-1,3-dioxolane
7965TJC6L6
NSC25480
AKOS015839253
phenyl acetaldehyde ethylene glycol acetal
B1404
CS-0325505
NS00013133
phenylacetaldehyde ethyleneglycol cyclic acetal
D88802
InChI=1/C10H12O2/c1-2-4-9(5-3-1)8-10-11-6-7-12-10/h1-5,10H,6-8H2