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CAS 175136-23-9

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2-(2,3-Dimethylphenoxy)-3-pyridinamine

Description:
2-(2,3-Dimethylphenoxy)-3-pyridinamine, identified by its CAS number 175136-23-9, is an organic compound characterized by its unique molecular structure, which includes a pyridine ring and a phenoxy group. This compound features a dimethyl-substituted phenyl moiety, contributing to its hydrophobic characteristics. The presence of the amino group (-NH2) on the pyridine ring enhances its potential for hydrogen bonding, which can influence its solubility and reactivity. Typically, compounds of this nature may exhibit biological activity, making them of interest in pharmaceutical research. The molecular interactions and properties can vary based on the substituents and their positions on the aromatic rings, affecting the compound's overall stability and reactivity. Additionally, the compound's synthesis and purification methods are crucial for obtaining it in a pure form for further study or application. As with many organic compounds, safety and handling precautions are essential due to potential toxicity or reactivity.
Formula:C13H14N2O
InChI:InChI=1S/C13H14N2O/c1-9-5-3-7-12(10(9)2)16-13-11(14)6-4-8-15-13/h3-8H,14H2,1-2H3
InChI key:InChIKey=PIQSAGQZHVNDSE-UHFFFAOYSA-N
SMILES:O(C1=C(C)C(C)=CC=C1)C2=C(N)C=CC=N2
Synonyms:
  • 2-(2,3-Dimethylphenoxy)pyridin-3-amine
  • 3-Pyridinamine, 2-(2,3-dimethylphenoxy)-
  • 2-(2,3-Dimethylphenoxy)-3-pyridinamine
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