2-Bromo-6-methyl-4-(trifluoromethyl)pyridine

95%

Reagent Code: #149858
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CAS Number 451459-17-9

science Other reagents with same CAS 451459-17-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 240.02 g/mol
Formula C₇H₅BrF₃N
badge Registry Numbers
MDL Number MFCD07368051
thermostat Physical Properties
Boiling Point 202.8°C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature, inert gas storage

description Product Description

Used as an intermediate in the synthesis of agrochemicals, particularly herbicides and insecticides, due to its halogen and electron-withdrawing trifluoromethyl group that enhance reactivity in cross-coupling reactions. Also employed in pharmaceutical research for building blocks in drug discovery, where the pyridine core contributes to biological activity and metabolic stability. Its structure allows for selective functionalization, making it valuable in creating complex molecules for crop protection and medicinal chemistry.

format_list_bulleted Product Specification

Test Parameter Specification
Appearance Colorless Liquid
Purity 94.5-100
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,350.00
inventory 5g
10-20 days ฿5,120.00
inventory 25g
10-20 days ฿21,600.00
inventory 100g
10-20 days ฿80,000.00

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2-Bromo-6-methyl-4-(trifluoromethyl)pyridine
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Used as an intermediate in the synthesis of agrochemicals, particularly herbicides and insecticides, due to its halogen and electron-withdrawing trifluoromethyl group that enhance reactivity in cross-coupling reactions. Also employed in pharmaceutical research for building blocks in drug discovery, where the pyridine core contributes to biological activity and metabolic stability. Its structure allows for selective functionalization, making it valuable in creating complex molecules for crop protection an

Used as an intermediate in the synthesis of agrochemicals, particularly herbicides and insecticides, due to its halogen and electron-withdrawing trifluoromethyl group that enhance reactivity in cross-coupling reactions. Also employed in pharmaceutical research for building blocks in drug discovery, where the pyridine core contributes to biological activity and metabolic stability. Its structure allows for selective functionalization, making it valuable in creating complex molecules for crop protection and medicinal chemistry.

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