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2-Bromoethyl acrylate

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Identification
Molecular formula
C5H7BrO2
CAS number
588-38-1
IUPAC name
2-bromoethyl prop-2-enoate
State
State

At room temperature, 2-bromoethyl acrylate is in a liquid state, which is typical for many organic esters of its kind. It should be handled with care as it may have hazardous vapors.

Melting point (Celsius)
-68.00
Melting point (Kelvin)
205.15
Boiling point (Celsius)
78.00
Boiling point (Kelvin)
351.15
General information
Molecular weight
180.01g/mol
Molar mass
180.0130g/mol
Density
1.5040g/cm3
Appearence

2-Bromoethyl acrylate is a colorless to yellowish liquid. Its appearance can vary slightly due to impurities, but it generally retains a clear to slightly yellow hue when pure.

Comment on solubility

Solubility of 2-bromoethyl prop-2-enoate

2-bromoethyl prop-2-enoate, with its chemical structure, presents some intriguing characteristics concerning its solubility. This compound, primarily known for its applications in organic synthesis, exhibits specific solubility behavior influenced by its molecular composition.

Generally, the solubility of 2-bromoethyl prop-2-enoate can be summarized as follows:

  • Polar solvents: The presence of the -Br atom and the ester group suggest that 2-bromoethyl prop-2-enoate shows greater solubility in polar solvents like alcohols and water. This enhanced solubility is due to the ability of the compound to form hydrogen bonds.
  • Non-polar solvents: Conversely, in non-polar solvents (such as hexane or toluene), the solubility may be considerably lower. The disparity in polarity can result in limited interaction between the solute and solvent molecules.
  • Temperature effect: In many cases, increasing the temperature may improve the solubility of 2-bromoethyl prop-2-enoate in various solvents, making it more accessible for chemical reactions.

As a conclusion, the solubility of 2-bromoethyl prop-2-enoate is heavily dependent on both its molecular structure and the nature of the solvent, illustrating the fascinating interplay between chemical properties and solubility phenomena. Understanding this relationship is crucial for effective application in both laboratory and industrial settings.

Interesting facts

Interesting Facts about 2-bromoethyl prop-2-enoate

2-bromoethyl prop-2-enoate is a fascinating compound that holds significant value in the realm of organic chemistry. Here are some notable aspects that highlight its importance:

  • Reactivity: As an alkyl halide, it can undergo various nucleophilic substitution reactions. This makes it a versatile building block for synthesizing more complex molecules.
  • Ester Linkage: The presence of the ester functional group in its structure provides the compound with unique chemical properties, such as participating in transesterification reactions, which are vital in the production of biodiesel.
  • Applications in Polymer Chemistry: 2-bromoethyl prop-2-enoate can serve as a monomer in the production of polymers. Its ability to undergo polymerization makes it a candidate for creating materials with specific properties, such as elasticity and strength.
  • Biological Activity: Research suggests that derivatives of 2-bromoethyl prop-2-enoate may exhibit interesting biological properties, which could lead to potential applications in drug development.
  • Synthesis: Scientists can synthesize this compound through various methods, including using alkylation reactions to introduce the bromo group, showcasing the principles of synthetic organic chemistry.

Studying 2-bromoethyl prop-2-enoate not only emphasizes the importance of functional groups in determining chemical behavior but also opens doors to innovative applications across various scientific fields. As chemists continue to explore its capabilities, the compound remains an intriguing subject of study.

Synonyms
2-BROMOETHYL ACRYLATE
Acrylic acid, 2-bromoethyl ester
CCRIS 4753
AI3-03834
NSC 18591
BRN 1749713
DTXSID4024648
DTXCID004648
ETHANOL, 2-BROMO-, ACRYLATE
4-02-00-01462 (beilstein handbook reference)
cdzaaihwzywbss-uhfffaoysa-n
4823-47-6
2-bromoethyl prop-2-enoate
2-Propenoic acid, 2-bromoethyl ester
Acrylic acid 2-bromoethyl ester
STU2P22H6X
acrylic acid 2-bromo-ethyl ester
NSC-18591
MFCD00013541
Bromoethyl acrylate, 2-
UNII-STU2P22H6X
SCHEMBL377483
2-Propenoicacid,2-bromoethylester
NSC18591
AKOS005207268
DB-051534
CS-0106645
E79074