5-Bromo-6-fluoro-7-iodo-1H-indole

95%

Reagent Code: #141427
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CAS Number 2891600-09-0

science Other reagents with same CAS 2891600-09-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 339.93 g/mol
Formula C₈H₄BrFIN
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry, light-proof

description Product Description

Used primarily as an intermediate in the synthesis of pharmaceuticals and biologically active compounds. Its halogen substituents allow selective cross-coupling reactions, making it valuable in medicinal chemistry for developing kinase inhibitors and receptor modulators. Commonly employed in research settings to construct complex indole-based scaffolds found in anticancer, antiviral, and anti-inflammatory agents. The presence of multiple halogens enables stepwise functionalization, facilitating structure-activity relationship studies. Also utilized in the development of fluorescent probes and imaging agents due to the indole core’s inherent photophysical properties.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿14,500.00
inventory 250mg
10-20 days ฿24,640.00
inventory 1g
10-20 days ฿66,510.00

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5-Bromo-6-fluoro-7-iodo-1H-indole
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Used primarily as an intermediate in the synthesis of pharmaceuticals and biologically active compounds. Its halogen substituents allow selective cross-coupling reactions, making it valuable in medicinal chemistry for developing kinase inhibitors and receptor modulators. Commonly employed in research settings to construct complex indole-based scaffolds found in anticancer, antiviral, and anti-inflammatory agents. The presence of multiple halogens enables stepwise functionalization, facilitating structure

Used primarily as an intermediate in the synthesis of pharmaceuticals and biologically active compounds. Its halogen substituents allow selective cross-coupling reactions, making it valuable in medicinal chemistry for developing kinase inhibitors and receptor modulators. Commonly employed in research settings to construct complex indole-based scaffolds found in anticancer, antiviral, and anti-inflammatory agents. The presence of multiple halogens enables stepwise functionalization, facilitating structure-activity relationship studies. Also utilized in the development of fluorescent probes and imaging agents due to the indole core’s inherent photophysical properties.

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