6-Bromo-7-methylquinoline

97%

Reagent Code: #145356
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CAS Number 122759-89-1

science Other reagents with same CAS 122759-89-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 222.08 g/mol
Formula C₁₀H₈BrN
badge Registry Numbers
MDL Number MFCD18260428
thermostat Physical Properties
Boiling Point 312.7±22.0°C
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used in the synthesis of pharmaceutical intermediates, particularly in the development of antimalarial and anticancer agents. Its structure serves as a key building block in heterocyclic chemistry, enabling the formation of complex quinoline-based compounds. It is also employed in research for creating novel organic materials and in the design of catalysts for cross-coupling reactions. Due to the presence of bromine, it readily participates in palladium-catalyzed reactions like Suzuki and Heck couplings, making it valuable in medicinal chemistry and drug discovery.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿760.00
inventory 1g
10-20 days ฿2,570.00
inventory 5g
10-20 days ฿11,930.00
inventory 10g
10-20 days ฿22,210.00

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6-Bromo-7-methylquinoline
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Used in the synthesis of pharmaceutical intermediates, particularly in the development of antimalarial and anticancer agents. Its structure serves as a key building block in heterocyclic chemistry, enabling the formation of complex quinoline-based compounds. It is also employed in research for creating novel organic materials and in the design of catalysts for cross-coupling reactions. Due to the presence of bromine, it readily participates in palladium-catalyzed reactions like Suzuki and Heck couplings,

Used in the synthesis of pharmaceutical intermediates, particularly in the development of antimalarial and anticancer agents. Its structure serves as a key building block in heterocyclic chemistry, enabling the formation of complex quinoline-based compounds. It is also employed in research for creating novel organic materials and in the design of catalysts for cross-coupling reactions. Due to the presence of bromine, it readily participates in palladium-catalyzed reactions like Suzuki and Heck couplings, making it valuable in medicinal chemistry and drug discovery.

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