3-Pyridinecarboxaldehyde, 2-amino-6-methyl- is an organic compound characterized by its pyridine ring structure, which features a carboxaldehyde functional group and an amino group. The presence of the amino group at the 2-position and the methyl group at the 6-position of the pyridine ring contributes to its unique chemical properties. This compound is typically a pale yellow to light brown solid or liquid, depending on its purity and specific conditions. It is soluble in polar solvents such as water and alcohols, which is indicative of its functional groups. The compound may exhibit biological activity, making it of interest in pharmaceutical and agrochemical research. Its reactivity is influenced by the electron-withdrawing nature of the aldehyde group and the electron-donating properties of the amino group, allowing for various chemical transformations. Additionally, it may participate in condensation reactions, nucleophilic substitutions, and other organic synthesis processes, making it a valuable intermediate in the synthesis of more complex molecules.

3-pyridinecarboxaldehyde, 2-amino-6-methyl-

885276-99-3: 2-Amino-6-methylnicotinaldehyde, 2-amino-6-methyl-Pyridinecarboxaldehyde

2-Amino-6-methylnicotinaldehyde

2-Amino-6-methyl-pyridine-3-carbaldehyde is a naphthyridine compound that has been shown to be a potent antagonist at the α2A receptor. It can also serve as an enantioselective synthesis intermediate for naphthyridines. The 2-amino group of this molecule is located on the opposite side of the 6-methyl group and is not involved in interactions with the receptor, which makes it an ideal candidate for use in analog syntheses. This compound has shown some potential as a pharmacological agent.

CAS 885276-99-3: 3-pyridinecarboxaldehyde, 2-amino-6-methyl-

2-Amino-6-methylnicotinaldehyde

Ref: 10-F225903

2-Amino-6-methyl-pyridine-3-carbaldehyde

Ref: 3D-FA148027

2-Amino-6-methylnicotinaldehyde

Ref: IN-DA0089B8