CAS 1532-25-8
:3,6-dichloropyridine-2-carboxamide
Description:
3,6-Dichloropyridine-2-carboxamide, with the CAS number 1532-25-8, is a chemical compound characterized by its pyridine ring structure, which is substituted at the 2, 3, and 6 positions. This compound features two chlorine atoms at the 3 and 6 positions of the pyridine ring and a carboxamide functional group at the 2 position. It is typically a solid at room temperature and is soluble in polar organic solvents. The presence of chlorine atoms contributes to its reactivity and potential applications in various chemical syntheses. This compound may exhibit biological activity, making it of interest in pharmaceutical research, particularly in the development of agrochemicals or medicinal compounds. Its molecular structure allows for interactions with biological targets, which can be explored for therapeutic purposes. As with many chlorinated compounds, it is essential to handle it with care due to potential toxicity and environmental concerns.
Formula:C6H4Cl2N2O
InChI:InChI=1/C6H4Cl2N2O/c7-3-1-2-4(8)10-5(3)6(9)11/h1-2H,(H2,9,11)
SMILES:c1cc(Cl)nc(c1Cl)C(=N)O
Synonyms:- 2-Pyridinecarboxamide, 3,6-Dichloro-
- 3,6-Dichlorpyridin-2-carboxamid
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Found 4 products.
3,6-Dichloropyridine-2-carboxamide
CAS:<p>3,6-Dichloropyridine-2-carboxamide</p>Formula:C6H4Cl2N2OPurity:≥95%Color and Shape: powderMolecular weight:191.01g/mol3,6-Dichloropicolinamide
CAS:<p>3,6-Dichloropicolinamide is a chemical compound with the molecular formula C5H4Cl2N2O. It belongs to the class of pyridine compounds. 3,6-Dichloropicolinamide is a potent inhibitor of cellular activity. The inhibition of synovial fibroblasts was shown using fluorescence and x-ray analysis. This chemical has also been shown to lower the solvents in human recombinant proteins and can be used as an alternative in these experiments.</p>Formula:C6H4Cl2N2OPurity:Min. 95%Molecular weight:191.01 g/mol
