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2-Bromoethyl acetate

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Identification
Molecular formula
C4H7BrO2
CAS number
927-68-4
IUPAC name
2-bromoethyl acetate
State
State

At room temperature, 2-bromoethyl acetate is a liquid. Its volatility and reactivity are typical of compounds containing both ester and alkyl bromide functional groups.

Melting point (Celsius)
-51.00
Melting point (Kelvin)
222.15
Boiling point (Celsius)
163.00
Boiling point (Kelvin)
436.15
General information
Molecular weight
167.00g/mol
Molar mass
167.0100g/mol
Density
1.4663g/cm3
Appearence

2-Bromoethyl acetate is a colorless to pale yellow liquid. It is an organic compound with a characteristic ester and bromide scent.

Comment on solubility

Solubility of 2-bromoethyl acetate

2-bromoethyl acetate, with the chemical formula C4H7BrO2, exhibits notable solubility characteristics that are important for various applications. The compound tends to be soluble in organic solvents due to its polar nature, while showing limited solubility in water. Here are a few key points regarding its solubility:

  • Solvent Compatibility: 2-bromoethyl acetate is typically soluble in common organic solvents such as ethanol, ether, and acetone.
  • Hydrophilicity vs. Hydrophobicity: Although it has an ester functional group, the presence of the bromine atom increases its hydrophobic characteristics, making it less soluble in water.
  • Temperature Dependence: As with many organic compounds, solubility can increase with temperature, allowing for better dissolution in organic solvents at elevated temperatures.

In summary, while 2-bromoethyl acetate is more compatible with non-polar or weakly polar solvents, it is wise to consider the implications of its limited solubility in aqueous environments for its practical uses. Understanding these solubility properties can be crucial for applications in chemical synthesis and formulation.

Interesting facts

Interesting Facts about 2-Bromoethyl Acetate

2-Bromoethyl acetate is a fascinating chemical compound known for its versatile applications in organic synthesis and its significance in various fields of chemistry. Here are some interesting aspects:

  • Functional Uses: This compound is commonly used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. Its ability to participate in a range of nucleophilic substitution reactions makes it a valuable building block in organic chemistry.
  • Reactivity: The presence of the bromine atom makes 2-bromoethyl acetate highly reactive. It can undergo reactions such as Williamson ether synthesis and can be converted into alcohols, amines, and more, showcasing its importance in creating diverse chemical entities.
  • Flavoring and Fragrance: Interestingly, esters like 2-bromoethyl acetate can contribute to the development of flavor and fragrance profiles in the food and cosmetic industries, proving its utility beyond strict chemical applications.
  • Environmental Concerns: As with many halogenated compounds, there are environmental and health considerations associated with the use of 2-bromoethyl acetate. It is crucial for researchers and practitioners to handle it with care and adhere to proper safety protocols due to potential toxicity.
  • Research and Innovation: Scientists are continually exploring novel applications for 2-bromoethyl acetate in the fields of material science and nanotechnology, showcasing its evolving relevance in modern research.

Quote from a chemist: "Understanding the behavior of 2-bromoethyl acetate opens up avenues for innovation in both synthetic methodologies and industrial applications."

In conclusion, the study of 2-bromoethyl acetate not only enhances our understanding of organic chemistry but also reflects the ever-evolving applications of such compounds in various scientific domains, underscoring their importance in both academic and practical settings.

Synonyms
2-BROMOETHYL ACETATE
927-68-4
Bromoethyl acetate
1-Acetoxy-2-bromoethane
2-Bromoethylacetate
1-Bromo-2-acetoxyethane
Ethanol, 2-bromo-, acetate
Acetic Acid 2-Bromoethyl Ester
2-acetoxyethyl bromide
2-bromoethanol acetate
Ethanol, 2-bromo-, 1-acetate
NSC 7079
EINECS 213-159-8
NRZ256O7QB
BRN 1743110
NSC-7079
BROMOETHYL ACETATE, 2-
DTXSID70878738
DTXCID401016777
213-159-8
MFCD00000235
Acetic acid 2-bromo-ethyl ester
UNII-NRZ256O7QB
bromoethylacetate
acetoxyethyl bromide
1-Acetoxy-2-bromoethane; 1-Bromo-2-acetoxyethane; 2-Acetoxyethyl Bromide; 2-Bromoethanol Acetate; Acetic Acid 2-Bromoethyl Ester; NSC 7079
(2-bromoethyl)acetate
2-acetyloxyethyl bromide
2-acetoxy-1-bromoethane
AcO-CH2-CH2-Br
2-bromoethan-1-ol acetate
2-Bromoethyl acetate, 97%
CHEMBL42088
SCHEMBL230055
NSC7079
AKOS015836240
CS-W007598
NCGC00166119-01
AS-14302
A0023
NS00042624
EN300-249904
Q27285024