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2-Bromoethyl hexanoate

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Identification
Molecular formula
C8H15BrO2
CAS number
4455-25-6
IUPAC name
2-bromoethyl hexanoate
State
State

At room temperature, 2-Bromoethyl hexanoate is a liquid. It is often stored in closed containers to avoid evaporation and exposure to air.

Melting point (Celsius)
-30.00
Melting point (Kelvin)
243.15
Boiling point (Celsius)
235.00
Boiling point (Kelvin)
508.15
General information
Molecular weight
223.11g/mol
Molar mass
223.0830g/mol
Density
1.1830g/cm3
Appearence

2-Bromoethyl hexanoate appears as a clear, colorless liquid. It may have a slightly oily texture due to its ester nature. Like most organic bromides, it can have a sharp and possibly unpleasant odor.

Comment on solubility

Solubility of 2-bromoethyl hexanoate

2-bromoethyl hexanoate, with the chemical formula C9H17BrO2, is an interesting compound in terms of solubility. Its solubility characteristics can be understood through the following points:

  • Polarity: The presence of the bromine atom and the ester functional group makes the molecule somewhat polar, which affects its interaction with solvents.
  • Solvent Compatibility: 2-bromoethyl hexanoate is likely to be soluble in organic solvents such as ethanol, acetone, and diethyl ether. However, its solubility in w waters will be limited due to its hydrophobic carbon chain.
  • Temperature Dependence: As with many organic compounds, solubility may increase with temperature, enhancing interactions with non-polar solvents.
  • Applications: Understanding the solubility of 2-bromoethyl hexanoate is crucial for its use in synthesis and reactions where solubility plays a key role.

As you can see, the solubility of 2-bromoethyl hexanoate demonstrates a balance between polar and non-polar characteristics. This makes it a compound that behaves predictably in organic solvents while being less compatible with polar solvents like water.

Interesting facts

Interesting Facts about 2-bromoethyl hexanoate

2-bromoethyl hexanoate is a fascinating compound in the realm of organic chemistry, known for its unique properties and versatile applications. Here are some key points that highlight its significance:

  • Structural Insights: This compound contains both a bromine atom and an ester functional group. The presence of bromine makes it highly reactive, offering a variety of pathways for further chemical transformations.
  • Applications in Synthesis: 2-bromoethyl hexanoate is often utilized as a building block in organic synthesis. It can serve as an intermediate in the preparation of other important compounds, facilitating the construction of complex molecular architectures.
  • Role in Polymerization: Due to its ability to undergo electrophilic substitution reactions, this compound can be employed in polymerization processes, contributing to the development of novel materials with desirable properties.
  • Biological Activities: Researchers have investigated the biological activities of various brominated esters, and compounds like 2-bromoethyl hexanoate may exhibit interesting interactions with biological systems, potentially leading to pharmaceutical applications.
  • Research Insights: The study of this compound can provide deeper insights into the behavior of brominated compounds in environmental chemistry, especially regarding how they interact with various substrates and their degradation pathways.

As with many organic compounds, safety precautions are crucial when handling 2-bromoethyl hexanoate. Proper laboratory practices ensure safety and efficiency during experimentation. As chemists continue to explore the potential of compounds like this, the future holds exciting possibilities for innovative applications.

Synonyms
2-Bromoethyl hexanoate
HEXANOIC ACID, 2-BROMOETHYL ESTER
6282-52-6
BRN 1756784
AI3-19988
DTXSID00211932
NSC 6984
DTXCID30134423
4-02-00-00922 (beilstein handbook reference)
ahelicbdmbdysn-uhfffaoysa-n
SCHEMBL11791792
NSC6984
NSC-6984
EN300-1478581