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2-Methoxy-1,3-dioxolane

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Identification
Molecular formula
C4H8O3
CAS number
4435-53-4
IUPAC name
2-methoxy-1,3-dioxolane
State
State

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

Melting point (Celsius)
-51.00
Melting point (Kelvin)
222.15
Boiling point (Celsius)
107.00
Boiling point (Kelvin)
380.15
General information
Molecular weight
104.11g/mol
Molar mass
104.1050g/mol
Density
1.0490g/cm3
Appearence

2-Methoxy-1,3-dioxolane is a colorless liquid.

Comment on solubility

Solubility of 2-methoxy-1,3-dioxolane

2-methoxy-1,3-dioxolane, with the molecular formula C5H10O3, exhibits interesting solubility characteristics that are important for various applications in chemical synthesis and processes.


Key Solubility Features:

  • Polar Nature: Due to the presence of oxygen atoms in its dioxolane structure, 2-methoxy-1,3-dioxolane possesses a degree of polarity, which generally enhances its solubility in polar solvents.
  • Water Solubility: This compound is relatively soluble in water, making it useful in aqueous reactions and formulations.
  • Solvent Compatibility: Additionally, it is soluble in organic solvents such as ethanol and acetone, which widens its applicability in organic synthesis.
  • Miscibility: Its ability to mix with various solvents without phase separation is a factor that enhances its versatility in laboratory and industrial settings.

In conclusion, the solubility of 2-methoxy-1,3-dioxolane contributes significantly to its utility in various chemical processes, making it an important compound to consider in both research and practical applications.

Interesting facts

Interesting Facts about 2-Methoxy-1,3-dioxolane

2-Methoxy-1,3-dioxolane is a fascinating compound with unique properties and applications in various fields of chemistry. Here are some intriguing points to consider:

  • Structure and Stability: The cyclic structure of 2-methoxy-1,3-dioxolane contributes to its stability. This compound features a five-membered ring that is resistant to certain types of chemical reactions, making it an ideal candidate for use in sensitive synthesis processes.
  • Solvent Uses: One of the primary applications of this compound is as a solvent. It is often used in reactions where a non-protic solvent is needed, providing non-reactive conditions that are crucial for the success of many chemical processes.
  • Role in Organic Synthesis: 2-Methoxy-1,3-dioxolane serves as a versatile reagent in organic synthesis. It enables various transformations due to its ability to function as both a nucleophile and an electrophile in different reaction conditions.
  • Its Applications: This compound finds applications in several areas, including:
    • As a building block in the synthesis of other complex organic molecules.
    • In the pharmaceutical industry for the preparation of drug intermediates.
    • In the field of polymer chemistry to develop new materials.
  • Environmental Considerations: Scientists are also exploring the environmental impact of this compound. While it is generally considered to have low toxicity, ongoing research aims to assess its biodegradability and overall environmental footprint.

In summary, 2-methoxy-1,3-dioxolane is more than just a compound; it plays a significant role in advancing both academic research and industrial processes. Its stability, versatility in synthesis, and practical applications make it an essential focus for chemists striving to innovate and expand the boundaries of chemical science.

Synonyms
2-METHOXY-1,3-DIOXOLANE
1,3-Dioxolane, 2-methoxy-
EINECS 243-229-3
VRAYTNFBRROPJU-UHFFFAOYSA-
DTXSID80173362
DTXCID8095853
243-229-3
InChI=1/C4H8O3/c1-5-4-6-2-3-7-4/h4H,2-3H2,1H3
RefChem:87794
VRAYTNFBRROPJU-UHFFFAOYSA-N
19693-75-5
MFCD00003208
SRV8DHN55D
SCHEMBL669092
SCHEMBL4912273
SCHEMBL28650675
2-Methoxy-1,3-dioxolane, 99%
1,3-Dioxolan-2-yl methyl ether #
AKOS015852556
AS-78330
DB-044944
M0816
NS00048264
D78408
EN300-187585