2-Amino-6-methylpyridine-3-carboxylic acid, also known by its CAS number 846021-26-9, is an organic compound characterized by its pyridine ring structure, which features an amino group and a carboxylic acid functional group. This compound typically exhibits properties associated with both basic and acidic functionalities due to the presence of the amino and carboxylic acid groups, respectively. It is a polar molecule, which enhances its solubility in water and other polar solvents. The methyl group at the 6-position of the pyridine ring contributes to its hydrophobic character, influencing its interactions in biological systems. This compound may participate in various chemical reactions, including nucleophilic substitutions and condensation reactions, making it of interest in synthetic organic chemistry. Additionally, its structural features suggest potential applications in pharmaceuticals, agrochemicals, or as a biochemical probe, although specific applications would depend on further research into its biological activity and reactivity.

2-amino-6-methylpyridine-3-carboxylic acid

846021-26-9: 2-Amino-6-methylnicotinic acid, 3-Pyridinecarboxylic Acid, 2-Amino-6-Methyl-

2-Amino-6-methylnicotinic acid

2-Amino-6-methyl-3-pyridinecarboxylic acid

2-Amino-6-methylnicotinic acid is a pharmaceutical drug which belongs to the class of organic solvents. It is used in the synthesis of nicotinamide and can be hydrolyzed into an acid ester. This product has been found to be an efficient reagent for the synthesis of amidines from amides and halides. 2-Amino-6-methylnicotinic acid is an important intermediate in agrochemical research and has been shown to have high yields during hydrolysis.

CAS 846021-26-9: 2-amino-6-methylpyridine-3-carboxylic acid

2-Amino-6-methylnicotinic acid

Ref: IN-DA004QAK

2-Amino-6-methylnicotinic acid

Ref: 54-OR90378

2-Amino-6-methyl-3-pyridinecarboxylic acid

Ref: 10-F331122

2-Amino-6-methylnicotinic acid

Ref: 3D-FA162120