CAS 53268-33-0
:2-Aminopyridine-5-thiocarboxamide
Description:
2-Aminopyridine-5-thiocarboxamide is an organic compound characterized by its pyridine ring, which is substituted with an amino group and a thiocarboxamide functional group. This compound typically exhibits properties associated with both amines and thiocarboxamides, such as potential basicity due to the amino group and reactivity stemming from the thiocarboxamide moiety. It is often used in various chemical synthesis processes, including the development of pharmaceuticals and agrochemicals, owing to its ability to participate in nucleophilic reactions. The presence of the thiocarboxamide group can enhance its reactivity in forming thioamide derivatives, which are valuable in medicinal chemistry. Additionally, 2-aminopyridine derivatives are known for their biological activities, including antimicrobial and anti-inflammatory properties. The compound is usually handled with standard laboratory precautions, as it may pose health risks if ingested or inhaled. Its solubility and stability can vary depending on the solvent and environmental conditions, making it important to consider these factors in practical applications.
Formula:C6H7N3S
InChI:InChI=1/C6H7N3S/c7-5-2-1-4(3-9-5)6(8)10/h1-3H,(H2,7,9)(H2,8,10)
SMILES:c1cc(=N)[nH]cc1C(=N)S
Synonyms:- 6-Aminopyridine-3-Carbothioamide
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Found 3 products.
6-Aminopyridine-3-thioamide
CAS:6-Aminopyridine-3-thioamide is a compound noted for its anticancer properties, capable of inhibiting the activity of specific enzymes that affect cell proliferation and survival. Furthermore, it has been studied for its potential to mitigate neurodegenerative diseases, exhibiting capabilities to enhance neural functions. The structural characteristics of 6-Aminopyridine-3-thioamide render it a significant bioactive molecule in compound development.Formula:C6H7N3SColor and Shape:SolidMolecular weight:153.21
