2-Iodo-6-(trifluoromethyl)pyridine

96%

Reagent Code: #199697
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CAS Number 100366-74-3

science Other reagents with same CAS 100366-74-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 272.99 g/mol
Formula C₆H₃F₃IN
thermostat Physical Properties
Melting Point 84-86°C
Boiling Point 206°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used primarily as an intermediate in the synthesis of pharmaceuticals and agrochemicals. Its structure allows for selective functionalization in cross-coupling reactions, making it valuable in the development of active ingredients in crop protection agents. Also employed in the preparation of kinase inhibitors and other biologically active compounds in medicinal chemistry research. The presence of iodine facilitates palladium-catalyzed reactions such as Suzuki or Heck couplings, enabling the construction of complex aromatic systems.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,120.00
inventory 1g
10-20 days ฿3,520.00
inventory 5g
10-20 days ฿14,590.00
2-Iodo-6-(trifluoromethyl)pyridine
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Used primarily as an intermediate in the synthesis of pharmaceuticals and agrochemicals. Its structure allows for selective functionalization in cross-coupling reactions, making it valuable in the development of active ingredients in crop protection agents. Also employed in the preparation of kinase inhibitors and other biologically active compounds in medicinal chemistry research. The presence of iodine facilitates palladium-catalyzed reactions such as Suzuki or Heck couplings, enabling the construction

Used primarily as an intermediate in the synthesis of pharmaceuticals and agrochemicals. Its structure allows for selective functionalization in cross-coupling reactions, making it valuable in the development of active ingredients in crop protection agents. Also employed in the preparation of kinase inhibitors and other biologically active compounds in medicinal chemistry research. The presence of iodine facilitates palladium-catalyzed reactions such as Suzuki or Heck couplings, enabling the construction of complex aromatic systems.

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