7-Bromo-3-methoxyquinoline

98%

Reagent Code: #152420
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CAS Number 1246548-95-7

science Other reagents with same CAS 1246548-95-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 238.08 g/mol
Formula C₁₀H₈BrNO
badge Registry Numbers
MDL Number MFCD18253949
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and antimalarial agents. Its structure supports the construction of complex heterocyclic systems found in bioactive molecules. Commonly employed in cross-coupling reactions such as Suzuki and Buchwald-Hartwig aminations to form carbon-carbon and carbon-nitrogen bonds, enabling the introduction of functional groups for drug optimization. Also utilized in the preparation of fluorescent probes and materials for organic electronics due to its quinoline backbone, which offers favorable photophysical properties.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿10,130.00
inventory 100mg
10-20 days ฿17,030.00
inventory 250mg
10-20 days ฿31,730.00

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7-Bromo-3-methoxyquinoline
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and antimalarial agents. Its structure supports the construction of complex heterocyclic systems found in bioactive molecules. Commonly employed in cross-coupling reactions such as Suzuki and Buchwald-Hartwig aminations to form carbon-carbon and carbon-nitrogen bonds, enabling the introduction of functional groups for drug optimization. Also utilized in the preparation of fluorescent probe

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and antimalarial agents. Its structure supports the construction of complex heterocyclic systems found in bioactive molecules. Commonly employed in cross-coupling reactions such as Suzuki and Buchwald-Hartwig aminations to form carbon-carbon and carbon-nitrogen bonds, enabling the introduction of functional groups for drug optimization. Also utilized in the preparation of fluorescent probes and materials for organic electronics due to its quinoline backbone, which offers favorable photophysical properties.

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