1,6-Naphthyridin-3-amine is a heterocyclic organic compound characterized by a fused bicyclic structure containing a nitrogen atom in its ring system. It features a naphthyridine core, which consists of a pyridine ring fused to another ring, contributing to its aromatic properties. The presence of an amino group (-NH2) at the 3-position of the naphthyridine enhances its reactivity and solubility in polar solvents. This compound is typically a solid at room temperature and may exhibit moderate to high stability under standard conditions. It is of interest in medicinal chemistry due to its potential biological activities, including antimicrobial and anticancer properties. The compound's molecular structure allows for various functionalizations, making it a versatile building block in the synthesis of more complex molecules. Additionally, its properties can be influenced by substituents on the aromatic rings, which can modulate its electronic characteristics and reactivity. As with many nitrogen-containing heterocycles, it may also participate in hydrogen bonding, affecting its interactions in biological systems.

1,6-Naphthyridin-3-amine

53454-30-1: 1,6-Naphthyridin-3-amine is a heterocyclic organic compound characterized by a fused bicyclic structure containing a nitrogen atom in its ring system. It features a naphthyridine core, which consists of a pyridine ring fused to another ring, contributing to its aromatic properties. The presence of an amino group (-NH2) at the 3-position of the naphthyridine enhances its reactivity and solubility in polar solvents. This compound is typically a solid at room temperature and may exhibit moderate to high stability under standard conditions. It is of interest in medicinal chemistry due to its potential biological activities, including antimicrobial and anticancer properties. The compound's molecular structure allows for various functionalizations, making it a versatile building block in the synthesis of more complex molecules. Additionally, its properties can be influenced by substituents on the aromatic rings, which can modulate its electronic characteristics and reactivity. As with many nitrogen-containing heterocycles, it may also participate in hydrogen bonding, affecting its interactions in biological systems.

CAS 53454-30-1

1,6-Naphthyridin-3-amine

1,6-Naphthyridin-3-amine

Ref: IN-DA00E3G7

1,6-Naphthyridin-3-amine

Ref: TR-N373540