2,3-dibromopropyl 2-methylprop-2-enoate

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Identification

Molecular formula
C7H10Br2O2
CAS Number
1604-43-7
IUPAC Name
2,3-dibromopropyl 2-methylprop-2-enoate
Molecular Weight
283.94g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
2.0240g/cm3
Synonyms
2, 3-Dibromopropyl methacrylate
Interesting facts

Interesting Facts about 2,3-Dibromopropyl 2-methylprop-2-enoate

2,3-Dibromopropyl 2-methylprop-2-enoate is a fascinating compound within the realm of organic chemistry. This compound is particularly noteworthy for the following reasons:

  • Reactivity: With its multiple bromine atoms, 2,3-dibromopropyl 2-methylprop-2-enoate showcases enhanced reactivity. The presence of bromine introduces electrophilic characteristics, making it an interesting subject for nucleophilic substitution reactions.
  • Applications: This compound finds potential applications in the synthesis of various polymers and may be used as a building block for more complex molecules. The presence of the acrylate group makes it suitable for use in UV-curable coatings and adhesives.
  • Stereochemistry: The compound's unique structure allows for stereochemical variations, which could lead to different isomeric forms. Each isomer may exhibit distinct physical and chemical properties, making studies on this compound particularly engaging.
  • Biological Significance: Similar compounds are often investigated for their biological activity. Understanding the behavior of brominated compounds can provide insights into their potential roles in pharmacology and agrochemical applications.
  • Synthesis Routes: The synthesis of 2,3-dibromopropyl 2-methylprop-2-enoate typically involves well-defined chemical pathways that are rich in mechanistic detail. This provides an excellent opportunity for students and chemists to explore reaction mechanisms and synthetic strategies.

In summary, 2,3-dibromopropyl 2-methylprop-2-enoate is not only a compound of theoretical interest but also holds substantial potential for practical applications in various fields. Understanding its properties and reactions can open new avenues in chemical research.

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