4,8-Dichloro-1,7-naphthyridine is a heterocyclic organic compound characterized by the presence of a naphthyridine ring system, which consists of a fused bicyclic structure containing nitrogen atoms. The specific substitution of chlorine atoms at the 4 and 8 positions contributes to its unique chemical properties, influencing its reactivity and potential applications. This compound typically exhibits a pale to dark solid appearance and is soluble in organic solvents. Its molecular structure suggests potential biological activity, making it of interest in pharmaceutical research, particularly in the development of antimicrobial or anticancer agents. The presence of chlorine atoms can enhance lipophilicity, affecting its bioavailability and interaction with biological targets. Additionally, 4,8-dichloro-1,7-naphthyridine may undergo various chemical reactions, including nucleophilic substitutions and electrophilic aromatic substitutions, which can be exploited in synthetic organic chemistry. Safety data should be consulted for handling and storage, as halogenated compounds can pose environmental and health risks.

4,8-dichloro-1,7-naphthyridine

1279894-03-9: 4,8-Dichloro-1,7-naphthyridine is a heterocyclic organic compound characterized by the presence of a naphthyridine ring system, which consists of a fused bicyclic structure containing nitrogen atoms. The specific substitution of chlorine atoms at the 4 and 8 positions contributes to its unique chemical properties, influencing its reactivity and potential applications. This compound typically exhibits a pale to dark solid appearance and is soluble in organic solvents. Its molecular structure suggests potential biological activity, making it of interest in pharmaceutical research, particularly in the development of antimicrobial or anticancer agents. The presence of chlorine atoms can enhance lipophilicity, affecting its bioavailability and interaction with biological targets. Additionally, 4,8-dichloro-1,7-naphthyridine may undergo various chemical reactions, including nucleophilic substitutions and electrophilic aromatic substitutions, which can be exploited in synthetic organic chemistry. Safety data should be consulted for handling and storage, as halogenated compounds can pose environmental and health risks.

CAS 1279894-03-9

4,8-dichloro-1,7-naphthyridine

1,7-Naphthyridine, 4,8-dichloro-

Ref: IN-DA000XMZ

4,8-Dichloro-1,7-naphthyridine

Ref: 54-OR1021639

4,8-Dichloro-1,7-naphthyridine

Ref: 10-F322423