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CAS 38875-53-5

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2,3-Diamino-5-bromopyridine

Description:
2,3-Diamino-5-bromopyridine is an organic compound characterized by its pyridine ring, which is substituted with two amino groups and one bromine atom. The presence of the amino groups (-NH2) at the 2 and 3 positions of the pyridine ring contributes to its basicity and potential reactivity, making it a versatile intermediate in organic synthesis. The bromine atom at the 5 position introduces a halogen functionality, which can participate in various chemical reactions, such as nucleophilic substitutions or coupling reactions. This compound is typically a solid at room temperature and may exhibit moderate solubility in polar solvents due to the presence of the amino groups. Its molecular structure allows for potential applications in pharmaceuticals, agrochemicals, and materials science, particularly in the development of dyes or ligands. Safety data should be consulted, as the compound may pose health risks if not handled properly, and appropriate safety measures should be taken during its use in laboratory settings.
Formula:C5H6BrN3
InChI:InChI=1S/C5H6BrN3/c6-3-1-4(7)5(8)9-2-3/h1-2H,7H2,(H2,8,9)
InChI key:InChIKey=YRGMYJUKFJPNPD-UHFFFAOYSA-N
SMILES:NC1=C(N)N=CC(Br)=C1
Synonyms:
  • 2,3-Diamino-5-Bromopyridinium
  • 2,3-Diamino-5-bromopyridine
  • 2,3-Pyridinediamine, 5-bromo-
  • 5-Bromo-2,3-pyridinediamine
  • 5-Bromopyridine-2,3-diamine
  • Pyridine, 2,3-diamino-5-bromo-
  • 5-Bromo-2,3-diaminopyridine
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