4'-Bromoacetophenone

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Identification

Molecular formula
C8H7BrNO
CAS Number
99-90-1
IUPAC Name
2-amino-1-(4-bromophenyl)ethanone
Molecular Weight
199.05g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.5100g/cm3
Synonyms
2-amino-1-(4-bromophenyl)ethanone
Interesting facts

Interesting Facts about 2-amino-1-(4-bromophenyl)ethanone

2-amino-1-(4-bromophenyl)ethanone, often abbreviated as ABPE, is a fascinating compound that has garnered attention in various fields, particularly in medicinal chemistry. Here are some intriguing aspects of this compound:

  • Pharmacological Interest: ABPE has been studied for its potential biological activities, demonstrating significant promise in drug development, particularly as an anti-cancer agent.
  • Structural Features: The presence of the bromine atom in the para position of the phenyl ring enhances the compound's electrophilic characteristics, potentially influencing its reactivity and biological interactions.
  • Amino Group Significance: The amino group attached to the ethanone carbon serves as an important functional site, which can participate in hydrogen bonding and contribute to the compound's solubility and interaction with biological molecules.
  • Synthetic Routes: There are various synthetic methods to obtain ABPE, which often involve substitution reactions. Understanding these pathways is crucial for developing more efficient synthesis strategies in the laboratory.
  • Research Applications: Beyond its pharmacological potential, ABPE is utilized in organic synthesis as a building block for constructing complex molecules in chemical research.

"Understanding compounds like 2-amino-1-(4-bromophenyl)ethanone is essential for advancing the field of organic and medicinal chemistry."

Its wide array of applications makes 2-amino-1-(4-bromophenyl)ethanone a compound worth exploring for researchers and students alike. The interplay between its structure and biological activity continues to be a rich area for further investigation.

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