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2-Ethyl-1,3,2-dioxaborolane

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Identification
Molecular formula
C4H9BO2
CAS number
4435-51-8
IUPAC name
2-ethyl-1,3,2-dioxaborolane
State
State

At room temperature, 2-ethyl-1,3,2-dioxaborolane is in a liquid state. It is used in various chemical processes and as a reagent in laboratory settings.

Melting point (Celsius)
-60.00
Melting point (Kelvin)
213.15
Boiling point (Celsius)
107.00
Boiling point (Kelvin)
380.15
General information
Molecular weight
100.93g/mol
Molar mass
100.9300g/mol
Density
1.0220g/cm3
Appearence

2-Ethyl-1,3,2-dioxaborolane typically appears as a colorless liquid. It is often used in organic synthesis, especially as a protecting group for diols.

Comment on solubility

Solubility of 2-ethyl-1,3,2-dioxaborolane (C4H9BO2)

2-ethyl-1,3,2-dioxaborolane, often referred to as a dioxaborolane derivative, exhibits intriguing solubility characteristics. Its solubility is primarily influenced by its polar nature and the presence of both the boron atom and the dioxaborolane structure. Here are some key points regarding its solubility:

  • Polar Solvent Compatibility: This compound is generally soluble in polar solvents such as water and alcohols, due to its ability to form hydrogen bonds and its polar functional groups.
  • Solubility in Non-Polar Solvents: In contrast, it exhibits limited solubility in non-polar solvents like hexane or benzene, as the molecule lacks significant hydrophobic interactions.
  • Temperature Effects: Solubility can also be affected by temperature; typically, higher temperatures may enhance solubility in polar solvents.

As with many chemical compounds, the solubility of 2-ethyl-1,3,2-dioxaborolane can be contingent on various factors, such as pH and the presence of different solutes. Thus, while this compound shows strong compatibility with polar media, it is essential to consider these variables when assessing its solubility in different environments.

Interesting facts

Interesting Facts about 2-Ethyl-1,3,2-Dioxaborolane

2-Ethyl-1,3,2-dioxaborolane is a fascinating compound that belongs to the family of boron-containing compounds. Its unique structure and properties make it noteworthy in various fields, particularly in organometallic chemistry and materials science.

Key Characteristics

  • Reactivity: This compound exhibits interesting reactivity patterns, attributable to the presence of boron. It can participate in various chemical reactions such as cross-coupling reactions, which are essential in organic synthesis.
  • Functional Group: The dioxaborolane ring structure includes a dual oxygen environment that imparts distinctive properties, aiding in the stabilization of reactive intermediates.
  • Versatility: This compound is often used as a boron source in the formation of boronic acids, which are crucial for the construction of complex organic molecules.

Applications

2-Ethyl-1,3,2-dioxaborolane has found numerous applications across various industries:

  • Pharmaceuticals: Its ability to form stable intermediates makes it ideal for drug discovery processes.
  • Polymer Science: This compound can be used to create boron-containing polymers that may possess unique thermal and mechanical properties.
  • Catalysis: It serves as a catalyst or catalyst precursor in several synthetic pathways.

Conclusion

In summary, 2-ethyl-1,3,2-dioxaborolane is more than just a chemical compound; it is a tool in advancing modern chemistry. Its reactivity, versatility, and wide range of applications make it an exciting subject for both scientists and students alike.


Synonyms
2-ETHYL-1,3,2-DIOXABOROLANE
10173-38-3
1,3,2-Dioxaborolane, 2-ethyl-
Ethaneboronic acid, cyclic ethylene ester
Cyclic ethylene ethylboronate
SCHEMBL735936
DTXSID00144150
2-Ethyl-1,3,2-dioxaborolane #
InChI=1/C4H9BO2/c1-2-5-6-3-4-7-5/h2-4H2,1H