3-Bromo-2-(trifluoromethoxy)pyridine

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Reagent Code: #117943
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CAS Number 1086393-00-1

science Other reagents with same CAS 1086393-00-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 241.99 g/mol
Formula C₆H₃BrF₃NO
badge Registry Numbers
MDL Number MFCD11506285
thermostat Physical Properties
Boiling Point 151.6±35.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature, away from light, stored in an inert gas

description Product Description

This chemical is primarily used as an intermediate in the synthesis of more complex compounds, particularly in the pharmaceutical and agrochemical industries. Its structure, featuring both bromine and trifluoromethoxy groups, makes it valuable for creating molecules with specific biological activities. In pharmaceuticals, it is often employed in the development of active ingredients for drugs targeting neurological disorders, inflammation, or infectious diseases. In agrochemicals, it serves as a building block for the production of pesticides or herbicides, where the trifluoromethoxy group can enhance the compound’s stability and efficacy. Additionally, its unique reactivity allows for further functionalization, making it a versatile component in organic synthesis and research applications.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿19,908.00
inventory 250mg
10-20 days ฿35,829.00

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3-Bromo-2-(trifluoromethoxy)pyridine
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This chemical is primarily used as an intermediate in the synthesis of more complex compounds, particularly in the pharmaceutical and agrochemical industries. Its structure, featuring both bromine and trifluoromethoxy groups, makes it valuable for creating molecules with specific biological activities. In pharmaceuticals, it is often employed in the development of active ingredients for drugs targeting neurological disorders, inflammation, or infectious diseases. In agrochemicals, it serves as a building block for the production of pesticides or herbicides, where the trifluoromethoxy group can enhance the compound’s stability and efficacy. Additionally, its unique reactivity allows for further functionalization, making it a versatile component in organic synthesis and research applications.
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