5-Bromo-2-(trifluoromethoxy)pyridine

98%

Reagent Code: #152067
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CAS Number 886371-77-3

science Other reagents with same CAS 886371-77-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 241.99 g/mol
Formula C₆H₃BrF₃NO
badge Registry Numbers
MDL Number MFCD07374891
thermostat Physical Properties
Boiling Point 157.1 °C at 760 mmHg
inventory_2 Storage & Handling
Storage -20°C, Inert Gas

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of agrochemicals and active ingredients in crop protection products. Its structure supports the creation of complex molecules with enhanced biological activity. Commonly employed in cross-coupling reactions such as Suzuki and Negishi couplings to build biaryl systems in drug discovery. Also utilized in the preparation of kinase inhibitors and other bioactive compounds due to the presence of bromine and electron-withdrawing trifluoromethoxy group, which facilitate selective functionalization.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿4,000.00
inventory 100mg
10-20 days ฿6,550.00
inventory 250mg
10-20 days ฿13,180.00
inventory 1g
10-20 days ฿40,650.00
inventory 5g
10-20 days ฿129,270.00

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5-Bromo-2-(trifluoromethoxy)pyridine
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of agrochemicals and active ingredients in crop protection products. Its structure supports the creation of complex molecules with enhanced biological activity. Commonly employed in cross-coupling reactions such as Suzuki and Negishi couplings to build biaryl systems in drug discovery. Also utilized in the preparation of kinase inhibitors and other bioactive compounds due to the presence of bromine and electro

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of agrochemicals and active ingredients in crop protection products. Its structure supports the creation of complex molecules with enhanced biological activity. Commonly employed in cross-coupling reactions such as Suzuki and Negishi couplings to build biaryl systems in drug discovery. Also utilized in the preparation of kinase inhibitors and other bioactive compounds due to the presence of bromine and electron-withdrawing trifluoromethoxy group, which facilitate selective functionalization.

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