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CAS 321845-13-0

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5-Amino-6-chloro-3-pyridinemethanol

Description:
5-Amino-6-chloro-3-pyridinemethanol is an organic compound characterized by its pyridine ring structure, which contains both an amino group and a hydroxymethyl group. The presence of the amino group (-NH2) suggests that it can participate in various chemical reactions, including nucleophilic substitutions and coupling reactions. The chloro substituent at the 6-position of the pyridine ring introduces reactivity, allowing for further derivatization. This compound is typically a solid at room temperature and may exhibit moderate solubility in polar solvents due to the hydroxymethyl group. Its molecular structure indicates potential applications in pharmaceuticals, particularly in the development of biologically active compounds, as the pyridine moiety is often found in many drugs. Additionally, the compound's properties, such as melting point, boiling point, and spectral characteristics, can be influenced by the functional groups present, making it a subject of interest in synthetic organic chemistry and medicinal chemistry research.
Formula:C6H7ClN2O
InChI:InChI=1S/C6H7ClN2O/c7-6-5(8)1-4(3-10)2-9-6/h1-2,10H,3,8H2
InChI key:InChIKey=WCUMYTNCDWNIHS-UHFFFAOYSA-N
SMILES:C(O)C=1C=C(N)C(Cl)=NC1
Synonyms:
  • (5-Amino-6-chloropyridin-3-yl)methanol
  • 3-Pyridinemethanol, 5-amino-6-chloro-
  • 5-Amino-6-chloro-3-pyridinemethanol
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