7-Bromo-2-methoxyquinoline is an organic compound characterized by its quinoline structure, which consists of a fused benzene and pyridine ring. The presence of a bromine atom at the 7-position and a methoxy group at the 2-position contributes to its unique chemical properties. This compound typically appears as a solid and is soluble in organic solvents. It exhibits notable reactivity due to the electron-withdrawing nature of the bromine atom, which can influence its electrophilic substitution reactions. The methoxy group, being an electron-donating substituent, can also affect the compound's reactivity and stability. 7-Bromo-2-methoxyquinoline is of interest in various fields, including medicinal chemistry, where it may serve as a precursor for the synthesis of biologically active compounds or as a potential pharmacophore in drug development. Its specific interactions and applications can vary based on the functional groups present and the overall molecular structure, making it a subject of study in both synthetic and applied chemistry.

7-Bromo-2-methoxyquinoline

99455-08-0: 7-Bromo-2-methoxyquinoline, Quinoline, 7-bromo-2-methoxy-

Quinoline, 7-bromo-2-methoxy-

7-Bromo-2-methoxyquinoline is a quinoline derivative that is structurally similar to the antiproliferative compounds vincristine and vinblastine. It has been shown to have good activity against solid cancer cells in culture, as well as being able to inhibit the proliferation of human breast cancer cell lines. 7-Bromo-2-methoxyquinoline has also been found to be cytotoxic to human fibroblasts, which may be due to its ability to inhibit DNA synthesis.

CAS 99455-08-0: 7-Bromo-2-methoxyquinoline

Quinoline, 7-bromo-2-methoxy-

Ref: IN-DA00IKAG

7-Bromo-2-methoxyquinoline

Ref: 54-OR75677

7-Bromo-2-methoxyquinoline

Ref: 10-F244206

7-Bromo-2-methoxyquinoline

Ref: 3D-FB142486