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CAS 4635-08-9

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5-Bromo-3,4-pyridinediamine

Description:
5-Bromo-3,4-pyridinediamine, with the CAS number 4635-08-9, is an organic compound characterized by its pyridine ring structure substituted with a bromine atom and two amino groups. This compound typically appears as a solid and is soluble in polar solvents, reflecting its ability to engage in hydrogen bonding due to the presence of amino groups. The bromine substitution introduces a halogen, which can influence the compound's reactivity and potential applications in synthesis. 5-Bromo-3,4-pyridinediamine is often utilized in medicinal chemistry and material science, serving as a building block for various pharmaceuticals and agrochemicals. Its reactivity can be attributed to the electron-withdrawing nature of the bromine atom, which can affect nucleophilic substitution reactions. Additionally, the amino groups can participate in various chemical reactions, including coupling reactions and the formation of more complex structures. Overall, this compound's unique structure and functional groups make it a valuable intermediate in organic synthesis.
Formula:C5H6BrN3
InChI:InChI=1S/C5H6BrN3/c6-3-1-9-2-4(7)5(3)8/h1-2H,7H2,(H2,8,9)
InChI key:InChIKey=CMFSWSZEHYPECE-UHFFFAOYSA-N
SMILES:NC=1C(Br)=CN=CC1N
Synonyms:
  • 3,4-Pyridinediamine, 5-Bromo-
  • 3-Bromopyridine-4,5-diamine
  • 5-Bromo-3,4-diaminepyridine
  • 5-Bromo-3,4-diaminopyridine
  • 5-Bromo-3,4-pyridinediamine
  • Pyridine, 3,4-diamino-5-bromo-
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