3-Bromo-6-(trifluoromethyl)imidazo[1,2-a]pyridine

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Reagent Code: #149998
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CAS Number 1146615-86-2

science Other reagents with same CAS 1146615-86-2

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scatter_plot Molecular Information
Weight 265.03 g/mol
Formula C₈H₄BrF₃N₂
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MDL Number MFCD12827771
inventory_2 Storage & Handling
Storage 2-8°C, avoid light, inert gas storage

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and anxiolytic agents. Its structure supports binding to specific enzyme active sites, making it valuable in drug discovery for neurological and oncological therapies. Also employed in agrochemical research for designing novel pesticides due to its stability and reactivity in cross-coupling reactions. Commonly utilized in Suzuki and Buchwald-Hartwig reactions to build complex heterocyclic systems in medicinal chemistry.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,660.00
inventory 5g
10-20 days ฿8,270.00
inventory 25g
10-20 days ฿24,380.00

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3-Bromo-6-(trifluoromethyl)imidazo[1,2-a]pyridine
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Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and anxiolytic agents. Its structure supports binding to specific enzyme active sites, making it valuable in drug discovery for neurological and oncological therapies. Also employed in agrochemical research for designing novel pesticides due to its stability and reactivity in cross-coupling reactions. Commonly utilized in Suzuki and Buchwald-Hartwig reactions to build complex hete

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and anxiolytic agents. Its structure supports binding to specific enzyme active sites, making it valuable in drug discovery for neurological and oncological therapies. Also employed in agrochemical research for designing novel pesticides due to its stability and reactivity in cross-coupling reactions. Commonly utilized in Suzuki and Buchwald-Hartwig reactions to build complex heterocyclic systems in medicinal chemistry.

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