1,6-Naphthyridin-5-amine is a heterocyclic organic compound characterized by its bicyclic structure, which consists of a naphthyridine ring system with an amino group (-NH2) at the 5-position. This compound typically exhibits properties associated with nitrogen-containing heterocycles, such as moderate solubility in polar solvents and potential for hydrogen bonding due to the presence of the amino group. It may display basicity due to the nitrogen atoms in the ring, which can participate in protonation reactions. The compound is of interest in medicinal chemistry and pharmaceutical research, as derivatives of naphthyridine are often explored for their biological activities, including antimicrobial and anticancer properties. Additionally, 1,6-Naphthyridin-5-amine can serve as a building block in the synthesis of more complex molecules. Its reactivity can be influenced by the presence of the amino group, allowing for various chemical transformations, such as acylation or alkylation. Overall, this compound represents a valuable structure in the development of new therapeutic agents.

1,6-Naphthyridin-5-amine

55570-60-0: 1,6-Naphthyridin-5-amine is a heterocyclic organic compound characterized by its bicyclic structure, which consists of a naphthyridine ring system with an amino group (-NH2) at the 5-position. This compound typically exhibits properties associated with nitrogen-containing heterocycles, such as moderate solubility in polar solvents and potential for hydrogen bonding due to the presence of the amino group. It may display basicity due to the nitrogen atoms in the ring, which can participate in protonation reactions. The compound is of interest in medicinal chemistry and pharmaceutical research, as derivatives of naphthyridine are often explored for their biological activities, including antimicrobial and anticancer properties. Additionally, 1,6-Naphthyridin-5-amine can serve as a building block in the synthesis of more complex molecules. Its reactivity can be influenced by the presence of the amino group, allowing for various chemical transformations, such as acylation or alkylation. Overall, this compound represents a valuable structure in the development of new therapeutic agents.

CAS 55570-60-0

1,6-Naphthyridin-5-amine

5-Amino-1,6-naphthyridine

Ref: IN-DA00DBJT

1,6-Naphthyridin-5-amine

Ref: 54-OR81970

1,6-Naphthyridin-5-amine

Ref: 10-F221258

1,6-Naphthyridin-5-amine

Ref: 3D-FCA57060