2-Chloro-5-methyl[1,6]naphthyridine is a heterocyclic organic compound characterized by its fused ring structure, which includes a naphthyridine moiety. This compound features a chlorine atom and a methyl group attached to the naphthyridine framework, influencing its chemical reactivity and physical properties. Typically, compounds of this type exhibit moderate to high lipophilicity due to their aromatic nature, which can affect their solubility in organic solvents. The presence of the chlorine atom can introduce electrophilic characteristics, making it a potential candidate for various chemical reactions, including nucleophilic substitutions. Additionally, the methyl group can affect the steric hindrance and electronic distribution within the molecule. Such compounds are often of interest in medicinal chemistry and material science due to their potential biological activity and utility in synthesizing more complex structures. As with many heterocycles, the specific properties, such as melting point, boiling point, and reactivity, can vary based on the substituents and the overall molecular structure.

2-CHLORO-5-METHYL[1,6]NAPHTHYRIDINE

140692-93-9: 2-Chloro-5-methyl[1,6]naphthyridine is a heterocyclic organic compound characterized by its fused ring structure, which includes a naphthyridine moiety. This compound features a chlorine atom and a methyl group attached to the naphthyridine framework, influencing its chemical reactivity and physical properties. Typically, compounds of this type exhibit moderate to high lipophilicity due to their aromatic nature, which can affect their solubility in organic solvents. The presence of the chlorine atom can introduce electrophilic characteristics, making it a potential candidate for various chemical reactions, including nucleophilic substitutions. Additionally, the methyl group can affect the steric hindrance and electronic distribution within the molecule. Such compounds are often of interest in medicinal chemistry and material science due to their potential biological activity and utility in synthesizing more complex structures. As with many heterocycles, the specific properties, such as melting point, boiling point, and reactivity, can vary based on the substituents and the overall molecular structure.

1,6-Naphthyridine, 2-chloro-5-methyl-

<p>2-Chloro-5-methyl-1,6-naphthyridine</p>

CAS 140692-93-9

2-CHLORO-5-METHYL[1,6]NAPHTHYRIDINE

1,6-Naphthyridine, 2-chloro-5-methyl-

Ref: IN-DA001COY

2-Chloro-5-methyl-1,6-naphthyridine

Ref: 54-OR32650

2-Chloro-5-methyl-1,6-naphthyridine

Ref: 10-F722456