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CAS 206997-15-1

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2-amino-5-bromopyridine-3-carbaldehyde

Description:
2-Amino-5-bromopyridine-3-carbaldehyde is an organic compound characterized by its pyridine ring, which is a six-membered aromatic heterocycle containing one nitrogen atom. This compound features an amino group (-NH2) and a bromine atom at the 5-position of the pyridine ring, while a formyl group (-CHO) is located at the 3-position. The presence of these functional groups imparts specific reactivity and properties to the molecule, making it useful in various chemical syntheses and applications, particularly in medicinal chemistry and the development of pharmaceuticals. The amino group can participate in nucleophilic reactions, while the aldehyde group is reactive towards nucleophiles, allowing for further derivatization. Additionally, the bromine atom can serve as a leaving group in substitution reactions. The compound is typically a solid at room temperature and may exhibit moderate solubility in polar solvents. Its unique structure and functional groups make it a valuable intermediate in the synthesis of more complex organic molecules.
Formula:C6H5BrN2O
InChI:InChI=1/C6H5BrN2O/c7-5-1-4(3-10)6(8)9-2-5/h1-3H,(H2,8,9)
SMILES:c1c(C=O)c(=N)[nH]cc1Br
Synonyms:
  • 2-Amino-5-bromo-3-pyridinecarboxaldehyde
  • 2-Amino-5-bromonicotinaldehyde
  • 2-Amino-5-bromopyridine-3-carboxaldehyde
  • 3-Pyridinecarboxaldehyde, 2-amino-5-bromo-
  • T6Nj Bz Cvh Ee
  • 2-Amino-5-bromopyridine-3-carbaldehyde
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