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: 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.

CAS 885276-99-3

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

2-Amino-6-methylnicotinaldehyde

Ref: IN-DA0089B8

2-Amino-6-methylnicotinaldehyde

Ref: 54-OR1032217

2-Amino-6-methylnicotinaldehyde

Ref: 10-F225903