5-Bromopicolinamide

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Identification

Molecular formula
C6H5BrN2O
CAS Number
5428-83-9
IUPAC Name
5-bromopyridine-3-carboxamide
Molecular Weight
201.03g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.7980g/cm3
Appearance
is typical of many organic compounds that contain halogenated benzene rings coupled with amide groups, which contribute to its solid state and crystalline structure.
Synonyms
5-bromonicotinamide
Interesting facts

Interesting Facts About 5-Bromopyridine-3-carboxamide

5-Bromopyridine-3-carboxamide is a fascinating compound, particularly noted for its utility in various fields of chemistry and medicinal applications. Below are some intriguing aspects of this compound:

  • Pyridine Derivative: As a member of the pyridine family, this compound features a nitrogen atom in its aromatic ring, which enhances its chemical reactivity and versatility.
  • Range of Applications: 5-Bromopyridine-3-carboxamide serves as a building block for numerous pharmaceuticals, agrochemicals, and fine chemicals, illustrating its importance in industrial chemistry.
  • Functional Groups: The presence of both a bromine atom and a carboxamide group lends this compound unique properties, making it an interesting subject for scientists exploring nucleophilic substitutions and other reactions.
  • Reactivity Insight: The bromine atom attached to the pyridine ring is known to enhance the electrophilicity of the adjacent functional groups, thereby influencing reaction pathways significantly.
  • Biological Relevance: Compounds analogous to 5-bromopyridine-3-carboxamide have shown potential in the design of inhibitors for various biological targets, making them crucial in drug discovery.

Overall, 5-bromopyridine-3-carboxamide stands out due to its structural features and myriad functional implications, making it a valuable compound in both research and application in chemistry. As the field of synthetic and medicinal chemistry continues to evolve, the importance of such compounds is only expected to grow.

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