5-Iodo-2-(trifluoromethyl)pyridine

98%

Reagent Code: #199784
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CAS Number 873107-98-3

science Other reagents with same CAS 873107-98-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 272.99 g/mol
Formula C₆H₃F₃IN
badge Registry Numbers
MDL Number MFCD11226772
thermostat Physical Properties
Melting Point 74-77°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used in pharmaceutical synthesis as an intermediate for active pharmaceutical ingredients, particularly in the development of kinase inhibitors, antimicrobials, anti-inflammatories, and other targeted therapies. Its structure supports cross-coupling reactions, making it valuable in forming carbon-carbon bonds during drug discovery. The iodine substituent acts as a directing group for substitution reactions, while the trifluoromethyl group provides electron-withdrawing properties, enhances molecular stability, and improves tissue solubility. Also employed in agrochemical research for designing novel pesticides due to these functional attributes. Suitable for use in palladium-catalyzed reactions such as Suzuki and Heck couplings.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿2,950.00
inventory 5g
10-20 days ฿10,870.00
inventory 10g
10-20 days ฿21,700.00
inventory 25g
10-20 days ฿54,200.00

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5-Iodo-2-(trifluoromethyl)pyridine
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Used in pharmaceutical synthesis as an intermediate for active pharmaceutical ingredients, particularly in the development of kinase inhibitors, antimicrobials, anti-inflammatories, and other targeted therapies. Its structure supports cross-coupling reactions, making it valuable in forming carbon-carbon bonds during drug discovery. The iodine substituent acts as a directing group for substitution reactions, while the trifluoromethyl group provides electron-withdrawing properties, enhances molecular stabi

Used in pharmaceutical synthesis as an intermediate for active pharmaceutical ingredients, particularly in the development of kinase inhibitors, antimicrobials, anti-inflammatories, and other targeted therapies. Its structure supports cross-coupling reactions, making it valuable in forming carbon-carbon bonds during drug discovery. The iodine substituent acts as a directing group for substitution reactions, while the trifluoromethyl group provides electron-withdrawing properties, enhances molecular stability, and improves tissue solubility. Also employed in agrochemical research for designing novel pesticides due to these functional attributes. Suitable for use in palladium-catalyzed reactions such as Suzuki and Heck couplings.

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