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CAS 1346691-32-4

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3-Chloro-5-(phenylmethoxy)pyridazine

Description:
3-Chloro-5-(phenylmethoxy)pyridazine is a chemical compound characterized by its pyridazine core, which is a six-membered aromatic ring containing two nitrogen atoms. The presence of a chlorine atom at the 3-position and a phenylmethoxy group at the 5-position contributes to its unique reactivity and potential applications in various fields, including pharmaceuticals and agrochemicals. The phenylmethoxy group enhances the compound's lipophilicity, potentially improving its bioavailability. This compound may exhibit interesting biological activities due to its structural features, making it a candidate for further research in medicinal chemistry. Its molecular structure suggests potential interactions with biological targets, and its chlorine substituent may influence its electronic properties and reactivity. As with many organic compounds, the stability, solubility, and reactivity of 3-Chloro-5-(phenylmethoxy)pyridazine can vary depending on environmental conditions and the presence of other functional groups. Safety and handling precautions should be observed, as with any chemical substance, to mitigate risks associated with its use.
Formula:C11H9ClN2O
InChI:InChI=1S/C11H9ClN2O/c12-11-6-10(7-13-14-11)15-8-9-4-2-1-3-5-9/h1-7H,8H2
InChI key:InChIKey=YMNJCWLKSHDYSE-UHFFFAOYSA-N
SMILES:O(CC1=CC=CC=C1)C=2C=C(Cl)N=NC2
Synonyms:
  • 3-Chloro-5-(phenylmethoxy)pyridazine
  • Pyridazine, 3-chloro-5-(phenylmethoxy)-
  • 5-(Benzyloxy)-3-chloropyridazine
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