2-Bromo-5-(trifluoromethoxy)pyridine

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Reagent Code: #144995
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CAS Number 888327-36-4

science Other reagents with same CAS 888327-36-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 241.99 g/mol
Formula C₆H₃BrF₃NO
thermostat Physical Properties
Boiling Point 194.1°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of agrochemicals and bioactive molecules. Its structure allows for selective functionalization, making it valuable in creating herbicides and insecticides. Commonly employed in cross-coupling reactions such as Suzuki or Heck reactions to build complex aromatic systems. Also utilized in the preparation of kinase inhibitors and other therapeutic agents due to the electron-withdrawing nature of the trifluoromethoxy group, which enhances metabolic stability and binding affinity in drug candidates.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,880.00
inventory 1g
10-20 days ฿5,680.00
inventory 500mg
10-20 days ฿3,600.00

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2-Bromo-5-(trifluoromethoxy)pyridine
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of agrochemicals and bioactive molecules. Its structure allows for selective functionalization, making it valuable in creating herbicides and insecticides. Commonly employed in cross-coupling reactions such as Suzuki or Heck reactions to build complex aromatic systems. Also utilized in the preparation of kinase inhibitors and other therapeutic agents due to the electron-withdrawing nature of the trifluorometho

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of agrochemicals and bioactive molecules. Its structure allows for selective functionalization, making it valuable in creating herbicides and insecticides. Commonly employed in cross-coupling reactions such as Suzuki or Heck reactions to build complex aromatic systems. Also utilized in the preparation of kinase inhibitors and other therapeutic agents due to the electron-withdrawing nature of the trifluoromethoxy group, which enhances metabolic stability and binding affinity in drug candidates.

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