6-(Benzyloxy)-3-bromoquinoline is an organic compound characterized by its quinoline backbone, which is a bicyclic structure containing a benzene ring fused to a pyridine ring. The presence of a bromine atom at the 3-position and a benzyloxy group at the 6-position contributes to its unique chemical properties. This compound is typically a solid at room temperature and may exhibit moderate solubility in organic solvents. Its structure suggests potential applications in medicinal chemistry, particularly in the development of pharmaceuticals, due to the biological activity often associated with quinoline derivatives. The bromine substituent can serve as a site for further chemical modifications, while the benzyloxy group may enhance lipophilicity, influencing the compound's interaction with biological systems. Additionally, the compound's reactivity can be influenced by the electron-withdrawing nature of the bromine atom and the electron-donating characteristics of the benzyloxy group, making it a versatile candidate for various synthetic pathways in organic chemistry.

6-(benzyloxy)-3-bromoquinoline

1337882-50-4: 6-(Benzyloxy)-3-bromoquinoline is an organic compound characterized by its quinoline backbone, which is a bicyclic structure containing a benzene ring fused to a pyridine ring. The presence of a bromine atom at the 3-position and a benzyloxy group at the 6-position contributes to its unique chemical properties. This compound is typically a solid at room temperature and may exhibit moderate solubility in organic solvents. Its structure suggests potential applications in medicinal chemistry, particularly in the development of pharmaceuticals, due to the biological activity often associated with quinoline derivatives. The bromine substituent can serve as a site for further chemical modifications, while the benzyloxy group may enhance lipophilicity, influencing the compound's interaction with biological systems. Additionally, the compound's reactivity can be influenced by the electron-withdrawing nature of the bromine atom and the electron-donating characteristics of the benzyloxy group, making it a versatile candidate for various synthetic pathways in organic chemistry.

CAS 1337882-50-4

6-(benzyloxy)-3-bromoquinoline

6-(Benzyloxy)-3-bromoquinoline

Ref: IN-DA00A010

6-(Benzyloxy)-3-bromoquinoline

Ref: 54-OR1004723

6-(Benzyloxy)-3-bromoquinoline

Ref: 10-F244764