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CAS 1614246-24-0

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5-Chloro-N3-ethyl-3,4-pyridazinediamine

Description:
5-Chloro-N3-ethyl-3,4-pyridazinediamine is a chemical compound characterized by its pyridazine core, which is a six-membered aromatic ring containing two nitrogen atoms. The presence of a chloro group at the 5-position and an ethyl substituent at the N3 position contributes to its unique reactivity and potential applications in medicinal chemistry. This compound may exhibit properties typical of amines, such as basicity and the ability to form hydrogen bonds, which can influence its solubility and interaction with biological targets. The structural features suggest potential for use in drug development, particularly in the synthesis of pharmaceuticals targeting specific biological pathways. Additionally, the presence of halogen and alkyl groups can enhance lipophilicity, affecting the compound's pharmacokinetics. As with many nitrogen-containing heterocycles, it may also participate in various chemical reactions, including nucleophilic substitutions and coupling reactions, making it a versatile building block in organic synthesis. Safety and handling considerations should be observed due to the presence of chlorine and the potential for biological activity.
Formula:C6H9ClN4
InChI:InChI=1S/C6H9ClN4/c1-2-9-6-5(8)4(7)3-10-11-6/h3H,2H2,1H3,(H2,8,10)(H,9,11)
InChI key:InChIKey=YCKYFDSKHUYUJC-UHFFFAOYSA-N
SMILES:N(CC)C1=C(N)C(Cl)=CN=N1
Synonyms:
  • 5-Chloro-N3-ethyl-3,4-pyridazinediamine
  • 3,4-Pyridazinediamine, 5-chloro-N3-ethyl-
  • 5-Chloro-N3-ethylpyridazine-3,4-diamine
  • 3,4-Pyridazinediamine 5-chloro-N3-ethyl-
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