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2-Isopropyl-1,3-dioxolane

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Identification
Molecular formula
C6H12O2
CAS number
6941-06-2
IUPAC name
2-isopropyl-1,3-dioxolane
State
State

2-Isopropyl-1,3-dioxolane is typically found as a liquid at room temperature.

Melting point (Celsius)
-42.50
Melting point (Kelvin)
230.60
Boiling point (Celsius)
115.30
Boiling point (Kelvin)
388.50
General information
Molecular weight
114.17g/mol
Molar mass
114.1730g/mol
Density
0.8450g/cm3
Appearence

2-Isopropyl-1,3-dioxolane is a colorless liquid that has a pleasant ether-like odor. It is a volatile compound and tends to evaporate quickly when exposed to the air.

Comment on solubility

Solubility of 2-Isopropyl-1,3-dioxolane

2-Isopropyl-1,3-dioxolane, known for its unique structural features, presents interesting solubility characteristics. Its solubility can be summarized as follows:

  • Polar Solvents: This compound is generally soluble in polar solvents such as water, due to the dioxolane ring which can form hydrogen bonds.
  • Non-Polar Solvents: Conversely, 2-isopropyl-1,3-dioxolane is also soluble in non-polar solvents like hexane, reflecting its hydrophobic isopropyl group.
  • Protic Solvents: Its solubility in protic solvents (e.g., alcohols) is favorable, enhancing its practical applications.

Overall, the solubility of 2-isopropyl-1,3-dioxolane varies significantly based on solvent polarity, making it a versatile compound in various chemical environments. As stated, "Solubility is the key to versatility," and this compound exemplifies that concept beautifully.

Interesting facts

Interesting Facts About 2-Isopropyl-1,3-dioxolane

2-Isopropyl-1,3-dioxolane is a fascinating organic compound that belongs to the class of dioxolanes—five-membered cyclic ethers characterized by the presence of two oxygen atoms in the ring. This compound is notable for its intriguing structure and distinct properties that make it valuable in various chemical applications.

Chemical Structure

  • The compound features a dioxolane ring, which is a cyclic ether structure that imparts unique physical and chemical characteristics.
  • The isopropyl group adds steric hindrance, influencing the compound's reactivity and stability.

Applications

2-Isopropyl-1,3-dioxolane finds applications in several fields:

  • Solvent: It is used as a solvent for various organic reactions due to its favorable solvent properties.
  • Chemical Synthesis: This compound serves as a key intermediate in the synthesis of more complex molecules, allowing chemists to access functional groups selectively.
  • Pharmaceuticals: Its structural attributes can lead to the development of new pharmaceuticals, enhancing drug formulations.

Unique Properties

Some compelling attributes of 2-isopropyl-1,3-dioxolane include:

  • It has a relatively low volatility, making it useful in applications where high stability is required.
  • The presence of the dioxolane ring contributes to its ability to stabilize reactive intermediates during chemical reactions.

Quote from the Field

As one chemist observed, "Understanding the structure of compounds like 2-isopropyl-1,3-dioxolane not only opens doors to innovative synthesis pathways but also sheds light on the fascinating behavior of cyclic ethers in organic chemistry."

In conclusion, 2-isopropyl-1,3-dioxolane is more than just a simple organic compound; it encapsulates the blend of theoretical chemistry and practical application in the realm of organic synthesis. Its unique structure and properties underscore the exciting possibilities available in modern chemical research.

Synonyms
2-ISOPROPYL-1,3-DIOXOLANE
1,3-Dioxolane, 2-isopropyl-
1,3-Dioxolane, 2-(1-methylethyl)-
2-Isopropyldioxolane
2-(propan-2-yl)-1,3-dioxolane
2-(1-Methylethyl)-1,3-dioxolane
CHEBI:87317
DTXSID50231620
NSC 139442
DTXCID80154111
inchi=1/c6h12o2/c1-5(2)6-7-3-4-8-6/h5-6h,3-4h2,1-2h
smyrhrfgkyucfb-uhfffaoysa-n
822-83-3
2-propan-2-yl-1,3-dioxolane
NSC-139442
NSC139442
1, 2-isopropyl-
AWV7Z4N6FJ
SCHEMBL3079746
AKOS006291982
ISOBUTYRALDEHYDE ETHYLENE ACETAL
DB-164468
Q27159520