8-Bromo-4-chloro-7-methylquinoline

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Reagent Code: #152358
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CAS Number 1388027-41-5

science Other reagents with same CAS 1388027-41-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 256.53 g/mol
Formula C₁₀H₇BrClN
badge Registry Numbers
MDL Number MFCD22560400
inventory_2 Storage & Handling
Storage Room temperature, inert gas

description Product Description

Used primarily as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of antimalarial and anticancer agents. Its halogenated structure allows for selective cross-coupling reactions, making it valuable in medicinal chemistry for building complex quinoline-based molecules. It is also employed in research settings to design kinase inhibitors and other biologically active compounds targeting specific cellular pathways. Due to the presence of bromo and chloro substituents, it serves as a versatile scaffold for sequential functionalization in drug discovery programs.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿9,480.00
inventory 250mg
10-20 days ฿16,120.00
inventory 1g
10-20 days ฿47,130.00

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8-Bromo-4-chloro-7-methylquinoline
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Used primarily as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of antimalarial and anticancer agents. Its halogenated structure allows for selective cross-coupling reactions, making it valuable in medicinal chemistry for building complex quinoline-based molecules. It is also employed in research settings to design kinase inhibitors and other biologically active compounds targeting specific cellular pathways. Due to the presence of bromo and chloro substitu

Used primarily as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of antimalarial and anticancer agents. Its halogenated structure allows for selective cross-coupling reactions, making it valuable in medicinal chemistry for building complex quinoline-based molecules. It is also employed in research settings to design kinase inhibitors and other biologically active compounds targeting specific cellular pathways. Due to the presence of bromo and chloro substituents, it serves as a versatile scaffold for sequential functionalization in drug discovery programs.

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