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2-isopropyl-2-methyl-1,3-dioxolane

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Identification
Molecular formula
C7H14O2
CAS number
50552-40-4
IUPAC name
2-isopropyl-2-methyl-1,3-dioxolane
State
State

At room temperature, 2-isopropyl-2-methyl-1,3-dioxolane exists as a liquid.

Melting point (Celsius)
-92.00
Melting point (Kelvin)
181.15
Boiling point (Celsius)
122.00
Boiling point (Kelvin)
395.15
General information
Molecular weight
130.19g/mol
Molar mass
130.1860g/mol
Density
0.9080g/cm3
Appearence

2-Isopropyl-2-methyl-1,3-dioxolane is a colorless liquid.

Comment on solubility

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

2-isopropyl-2-methyl-1,3-dioxolane is an intriguing compound with notable solubility characteristics. As a cyclic acetal, its solubility profile can be influenced by several factors:

  • Polarity: Being a Dioxolane, it possesses polar functional groups which generally enhance its solubility in polar solvents.
  • Water Solubility: Although 2-isopropyl-2-methyl-1,3-dioxolane is somewhat soluble in water, it is more soluble in organic solvents such as ethanol and diethyl ether.
  • Hydrophobic vs. Hydrophilic Balance: The presence of isopropyl and methyl groups contributes to a hydrophobic character, which may limit its overall solubility in highly polar solvents.
  • Temperature Effects: Like many compounds, its solubility may increase with temperature, making it more soluble in hot solvents compared to cold ones.

In practical applications, these solubility traits can be essential in determining the compound's behavior in various environments, influencing processes such as extraction and formulation.

Interesting facts

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

2-Isopropyl-2-methyl-1,3-dioxolane is a fascinating compound primarily known for its unique structure and functionality. Below are some intriguing insights into this compound:

  • Structural Features: The compound contains a dioxolane ring, which is a five-membered ring containing two oxygen atoms. This structure is a hallmark of several biologically relevant compounds.
  • Applications: It is often utilized as a solvent in organic synthesis and can serve as a building block in the preparation of other chemical derivatives. Its role as a solvent is attributed to its ability to dissolve various organic materials.
  • Reactivity: The presence of the dioxolane ring provides interesting reactivity patterns, especially in nucleophilic reactions. This can lead to various synthetic pathways that are crucial in developing new chemical compounds.
  • Biochemical Significance: Compounds with similar structures are often investigated for their potential biological activity. Researchers are continuously exploring their interactions within biological systems.

Quote from the Literature

As noted in chemical literature, "The unique properties of dioxolanes render them invaluable not just in synthetic chemistry but also in pharmaceuticals." This highlights the dual nature of dioxolanes, showcasing how they bridge synthetic methods with biological applications.

In summary, 2-Isopropyl-2-methyl-1,3-dioxolane is more than just a chemical compound; it represents a convergence of synthetic utility and potential biological significance. The continuous study of such compounds expands our understanding of chemistry and its various applications.

Synonyms
2-METHYL-2-ISOPROPYL-1,3-DIOXOLANE
4405-16-7
1,3-Dioxolane, 2-isopropyl-2-methyl-
1,3-Dioxolane, 2-methyl-2-(1-methylethyl)-
SCHEMBL777393
DTXSID30196026
2-Isopropyl-2-methyl-1,3-dioxolane #
1,3-DIOXOLANE, 2-METHYL-2-(1-METHYLETHYL)