3-Bromo-6-methoxyquinoline

96%

Reagent Code: #146525
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CAS Number 14036-96-5

science Other reagents with same CAS 14036-96-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 238.08 g/mol
Formula C₁₀H₈BrNO
badge Registry Numbers
MDL Number MFCD09260428
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 antimalarial and anticancer agents. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for building complex quinoline-based molecules. Commonly employed in cross-coupling reactions such as Suzuki and Heck reactions to form carbon-carbon bonds in drug discovery programs. Also utilized in the preparation of kinase inhibitors and antimicrobial compounds due to its ability to interact with biological targets.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿750.00
inventory 100mg
10-20 days ฿1,160.00
inventory 1g
10-20 days ฿8,590.00
inventory 250mg
10-20 days ฿2,210.00

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3-Bromo-6-methoxyquinoline
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of antimalarial and anticancer agents. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for building complex quinoline-based molecules. Commonly employed in cross-coupling reactions such as Suzuki and Heck reactions to form carbon-carbon bonds in drug discovery programs. Also utilized in the preparation of kinase inhibitors and antimicrobial compounds due to its a

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of antimalarial and anticancer agents. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for building complex quinoline-based molecules. Commonly employed in cross-coupling reactions such as Suzuki and Heck reactions to form carbon-carbon bonds in drug discovery programs. Also utilized in the preparation of kinase inhibitors and antimicrobial compounds due to its ability to interact with biological targets.

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