215113-43-2

Basic information

• Product Name: 1,3-Dioxolane,2-fluoro-4,4,5,5-tetramethyl-(9CI)
• Synonyms: 1,3-Dioxolane,2-fluoro-4,4,5,5-tetramethyl-(9CI)
• CAS NO: 215113-43-2
• Molecular Formula: C7H13FO2
• Molecular Weight: 148.1753232
• Product Categories: HALIDE
• Mol File: 215113-43-2.mol

Chemical Properties

• Boiling Point: 113.4±25.0 °C(Predicted)
• Appearance: /
• Density: 1.02±0.1 g/cm3(Predicted)
• CAS DataBase Reference: 1,3-Dioxolane,2-fluoro-4,4,5,5-tetramethyl-(9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3-Dioxolane,2-fluoro-4,4,5,5-tetramethyl-(9CI)(215113-43-2)
• EPA Substance Registry System: 1,3-Dioxolane,2-fluoro-4,4,5,5-tetramethyl-(9CI)(215113-43-2)

Safety Data

• Hazardous Substances Data: 215113-43-2(Hazardous Substances Data)

Usage

Structure

Five-membered cyclic ether ring with a fluorine atom and four methyl groups attached

Fluorinated derivative

Derived from dioxolane with the addition of a fluorine atom

Explanation

The compound is a fluorinated version of dioxolane, which means that a fluorine atom has been added to the dioxolane structure.

Explanation

The compound has various applications in the chemical industry and research, including its use as a solvent for various reactions and as a starting material for the synthesis of other organic compounds.

Explanation

The specific arrangement of atoms and the presence of a fluorine atom in the molecule give this compound unique properties that can be exploited in the development of new materials and pharmaceuticals.

Explanation

Due to its chemical nature, 1,3-Dioxolane,2-fluoro-4,4,5,5-tetramethyl-(9CI) requires careful handling and storage to ensure the safety of those working with it. This includes following established safety procedures and guidelines to minimize risks.

Industrial and research applications

Used as a solvent and building block in the synthesis of other organic compounds

Unique structure and properties

Useful in the development of new materials and pharmaceuticals

Safety precautions

Should be handled and stored with care, following proper safety procedures and guidelines

Upstream product

• 23011-88-3 4,4,5,5-tetramethyl-1,3-dioxolan-2-yl acetate 

Relevant articles and documents

Dimensiosolvatic effects. VI. Rates of ionization of 2-fluoro-4,4,5,5- tetramethyl-1,3-dioxolane: Dimensiosolvatic vs. hydrogen-bond effects

The title compound was prepared by treating 4,4,5,5-tetramethyl-1,3- dioxolan-2-yl acetate with cesium fluoride. Rates of ionization of this compound were determined in various solvents by the dynamic NMR technique. While effects due to polarity as well as solvent molecular size were observed in many solvents examined, the rates in solutions of which the solvent is capable of being an acceptor in hydrogen-bond formation with the substrate were unusually small, and this effect is diminished in bulky solvents. Such results are attributed to stabilization of the original state due to hydrogen-bond formation with the acidic C(2) - H group of the substrate in those solvents. The hydrogen-bond formation is hindered by the steric effects in bulkier solvents than in smaller solvents. The rates of contact ion pair and solvent-separated ion pair formations should be independently determined in 2-fluoro-4,4,5,5-tetramethyl-1,3-dioxolane, but so far no clear example which shows that the rate-limiting step is the solvent intervention has been found, even though various bulky solvents were examined.

2-Fluoro-4,4,5,5-tetramethyl-1,3-dioxolane: A compound carrying two independent probes for determining rates of formations of contact and solvent-separated ion pairs

2-Fluoro-4,4,5,5-tetramethyl-1,3-dioxolane was shown to be a useful compound for independently determining the rate constants of contact ion pair and solvent-separated ion pair formations. The compound was used to determine rate constants for toluene-d8 and chloroform-d solutions and they were found to be identical for each solution.