6-Bromo-4-iodoquinoline

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Reagent Code: #145587
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CAS Number 927801-23-8

science Other reagents with same CAS 927801-23-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 333.95 g/mol
Formula C₉H₅BrIN
badge Registry Numbers
MDL Number MFCD08437008
thermostat Physical Properties
Boiling Point 375.5°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used primarily as an intermediate in the synthesis of pharmaceuticals, particularly in the development of antimalarial and anticancer agents. Its halogenated structure allows for selective cross-coupling reactions, enabling the introduction of various functional groups during drug design. It is also employed in the preparation of quinoline-based fluorescent probes for biochemical imaging. Due to the presence of both bromo and iodo substituents, it offers sequential reactivity, making it valuable in multi-step organic synthesis for creating complex heterocyclic systems.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿610.00
inventory 250mg
10-20 days ฿1,130.00
inventory 1g
10-20 days ฿3,830.00
inventory 5g
10-20 days ฿12,050.00

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6-Bromo-4-iodoquinoline
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Used primarily as an intermediate in the synthesis of pharmaceuticals, particularly in the development of antimalarial and anticancer agents. Its halogenated structure allows for selective cross-coupling reactions, enabling the introduction of various functional groups during drug design. It is also employed in the preparation of quinoline-based fluorescent probes for biochemical imaging. Due to the presence of both bromo and iodo substituents, it offers sequential reactivity, making it valuable in multi

Used primarily as an intermediate in the synthesis of pharmaceuticals, particularly in the development of antimalarial and anticancer agents. Its halogenated structure allows for selective cross-coupling reactions, enabling the introduction of various functional groups during drug design. It is also employed in the preparation of quinoline-based fluorescent probes for biochemical imaging. Due to the presence of both bromo and iodo substituents, it offers sequential reactivity, making it valuable in multi-step organic synthesis for creating complex heterocyclic systems.

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