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CAS 912772-88-4

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3-Amino-2,6-dichloro-4-pyridinecarbonitrile

Description:
3-Amino-2,6-dichloro-4-pyridinecarbonitrile is a chemical compound characterized by its pyridine ring structure, which is substituted with an amino group, two chlorine atoms, and a cyano group. The presence of the amino group indicates that it can participate in hydrogen bonding, potentially enhancing its solubility in polar solvents. The dichloro substitutions contribute to its reactivity and may influence its biological activity, making it of interest in pharmaceutical research. The cyano group (nitrile) is known for its electron-withdrawing properties, which can affect the compound's overall reactivity and stability. This compound is typically synthesized through specific organic reactions that introduce the various functional groups onto the pyridine ring. Its unique structure may confer specific properties, such as antimicrobial or herbicidal activity, making it a candidate for various applications in medicinal chemistry and agrochemicals. As with many chemical substances, safety and handling precautions are essential due to potential toxicity or environmental impact.
Formula:C6H3Cl2N3
InChI:InChI=1S/C6H3Cl2N3/c7-4-1-3(2-9)5(10)6(8)11-4/h1H,10H2
InChI key:InChIKey=KHPTVQQHMHHJEZ-UHFFFAOYSA-N
SMILES:C(#N)C=1C(N)=C(Cl)N=C(Cl)C1
Synonyms:
  • 3-Amino-2,6-dichloro-4-pyridinecarbonitrile
  • 4-Pyridinecarbonitrile, 3-amino-2,6-dichloro-
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