CAS 152362-01-1
:2-chloro-4-methylpyridine-3-carboxamide
Description:
2-Chloro-4-methylpyridine-3-carboxamide is a chemical compound characterized by its pyridine ring structure, which includes a chlorine atom and a methyl group as substituents. The presence of the carboxamide functional group contributes to its polar nature, influencing its solubility in various solvents. This compound typically exhibits moderate stability under standard conditions but may be sensitive to strong acids or bases. Its molecular structure suggests potential applications in pharmaceuticals or agrochemicals, where the specific arrangement of functional groups can impart unique biological activities. The chlorine atom can enhance lipophilicity, while the carboxamide group may participate in hydrogen bonding, affecting the compound's reactivity and interaction with biological targets. Additionally, the compound's characteristics, such as melting point, boiling point, and spectral properties, can be determined through experimental methods, providing further insights into its behavior in different environments. Overall, 2-chloro-4-methylpyridine-3-carboxamide is a versatile compound with potential utility in various chemical applications.
Formula:C7H7ClN2O
Synonyms:- 3-Pyridinecarboxamide,2-chloro-4-methyl-
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Found 5 products.
2-Chloro-4-methylnicotinamide
CAS:Formula:C7H7ClN2OPurity:97%Color and Shape:SolidMolecular weight:170.59632-Chloro-4-methylnicotinamide
CAS:<p>2-Chloro-4-methylnicotinamide</p>Purity:95%Molecular weight:170.60g/mol2-Chloro-4-methylnicotinamide
CAS:Controlled Product<p>Applications 2-chloro-4-methylnicotinamide (cas# 152362-01-1) is a useful research chemical.<br></p>Formula:C7H7N2OClColor and Shape:NeatMolecular weight:170.62-Chloro-4-methylnicotinamide
CAS:<p>2-Chloro-4-methylnicotinamide is an element that has been used for medical purposes. It is a medication that has been shown to be effective against HIV, although it is not yet approved for this use. 2-Chloro-4-methylnicotinamide inhibits the transcriptase and reverse transcriptase of HIV by binding to the enzyme at specific sites in the active site. It also inhibits the activity of pyridines, which are enzymes that catalyze reactions in the body including DNA synthesis. This drug was developed with a partnership with Abbott Laboratories and is marketed as Nevirapine.<br>2-Chloro-4-methylnicotinamide can be found as an anhydrous salt or as a nonnucleoside analog of nevirapine.</p>Formula:C7H7ClN2OPurity:Min. 95%Molecular weight:170.6 g/mol




