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2-Methyl-2-propyl-1,3-dioxolane

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Identification
Molecular formula
C7H14O2
CAS number
141-79-7
IUPAC name
2-methyl-2-propyl-1,3-dioxolane
State
State

At room temperature, 2-Methyl-2-propyl-1,3-dioxolane is in a liquid state.

Melting point (Celsius)
-90.00
Melting point (Kelvin)
183.15
Boiling point (Celsius)
154.00
Boiling point (Kelvin)
427.15
General information
Molecular weight
130.19g/mol
Molar mass
130.1870g/mol
Density
0.8898g/cm3
Appearence

2-Methyl-2-propyl-1,3-dioxolane is generally a clear, colorless liquid with a slight, ether-like odor. Its refractive index indicates it may exhibit some light refraction under specific lighting conditions.

Comment on solubility

Solubility of 2-methyl-2-propyl-1,3-dioxolane

2-methyl-2-propyl-1,3-dioxolane, a cyclic ether, exhibits interesting solubility characteristics that stem from its molecular structure. Being a polar compound, it demonstrates variable solubility in different solvents:

  • Water: This compound has limited solubility in water due to its hydrophobic carbon chains, which hinder extensive interaction with water molecules.
  • Organic solvents: It shows a much higher solubility in organic solvents such as ethanol and acetone, which are compatible with its non-polar structure.

Generally, the solubility of 2-methyl-2-propyl-1,3-dioxolane in organic compounds indicates its behavior as a versatile solvent and potential usage in various chemical reactions.

In conclusion, the solubility range highlights the principle of "like dissolves like," where polar solvents can dissolve polar compounds effectively, while non-polar characteristics can limit solubility in water. The exploration of such properties is crucial for practical applications in the field of chemistry.

Interesting facts

Interesting Facts about 2-methyl-2-propyl-1,3-dioxolane

2-methyl-2-propyl-1,3-dioxolane, also known as an acetal, represents a fascinating class of organic compounds characterized by their unique structure and reactivity. This compound is significant for several reasons:

  • Synthetic Utility: Dioxolanes like 2-methyl-2-propyl-1,3-dioxolane are valuable intermediates in organic synthesis. They can be used for the protection of carbonyl compounds, thereby allowing for selective reactions in complex molecules.
  • Stability and Reactivity: The 1,3-dioxolane ring provides considerable chemical stability, and due to its reactive nature, can undergo hydrolysis under acidic conditions, which can lead to the generation of useful derivatives.
  • Potential Applications: These compounds are not only useful in academic research but also have implications in the pharmaceutical industry. They can serve as scaffolds or building blocks in drug discovery processes.
  • Historical Significance: The synthesis of dioxolanes was a noteworthy development in the field of organic chemistry, expanding the toolkit available to chemists for constructing more complex molecular architectures.

Furthermore, the fact that 2-methyl-2-propyl-1,3-dioxolane can easily be synthesized from readily available reagents makes it an attractive target for both students learning about organic reactions and seasoned chemists. The versatility of dioxolane structures opens a window into exploring innovative chemical reactions and product development.

In conclusion, 2-methyl-2-propyl-1,3-dioxolane stands as an exemplary compound illustrating the intersection of simplicity and functionality in organic chemistry. As noted by many chemists, "The beauty of chemistry lies not just in the compounds themselves, but in how we can manipulate them to create something new."

Synonyms
2-METHYL-2-PROPYL-1,3-DIOXOLANE
4352-98-1
DTXSID40195868
DTXCID80118359
1,3-Dioxolane, 2-methyl-2-propyl-
SCHEMBL2632837
NXGWCOIWOMWSDT-UHFFFAOYSA-N
2-Methyl-2-propyl-1,3-dioxolane #
2-Pentanone, cyclic 1,2-ethanediyl acetal