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CAS 175135-63-4

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2-(2,4-Difluorophenoxy)-3-pyridinamine

Description:
2-(2,4-Difluorophenoxy)-3-pyridinamine, with the CAS number 175135-63-4, is a chemical compound characterized by its unique molecular structure, which includes a pyridine ring and a difluorophenoxy group. This compound typically exhibits properties associated with both aromatic and heterocyclic compounds, such as stability and potential reactivity due to the presence of functional groups. The difluorophenoxy moiety can influence its solubility and polarity, while the pyridinamine part may contribute to its basicity and potential for hydrogen bonding. This compound may be of interest in medicinal chemistry, particularly for its potential biological activity, as many pyridine derivatives are known for their pharmacological properties. Additionally, the presence of fluorine atoms can enhance metabolic stability and lipophilicity, making it a candidate for further research in drug development. Overall, 2-(2,4-Difluorophenoxy)-3-pyridinamine represents a class of compounds that may have significant applications in various fields, including pharmaceuticals and agrochemicals.
Formula:C11H8F2N2O
InChI:InChI=1S/C11H8F2N2O/c12-7-3-4-10(8(13)6-7)16-11-9(14)2-1-5-15-11/h1-6H,14H2
InChI key:InChIKey=LCPVQAHEFVXVKT-UHFFFAOYSA-N
SMILES:O(C1=C(F)C=C(F)C=C1)C2=C(N)C=CC=N2
Synonyms:
  • 2-(2,4-Difluorophenoxy)-3-pyridinamine
  • 2-(2,4-Difluorophenoxy)pyridin-3-amine
  • 2-(4-Fluorophenoxy)Pyridin-3-Amine
  • 3-Pyridinamine, 2-(2,4-difluorophenoxy)-
  • 3-Amino-2-(2,4-difluorophenoxy)pyridine
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