4-Iodo-2-(trifluoromethyl)pyridine

97%

Reagent Code: #199698
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CAS Number 590371-73-6

science Other reagents with same CAS 590371-73-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 272.99 g/mol
Formula C₆H₃F₃IN
thermostat Physical Properties
Melting Point 24-26°C
Boiling Point 206°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 kinase inhibitors and other bioactive molecules. Its structure allows for selective cross-coupling reactions, making it valuable in medicinal chemistry for building complex heterocyclic compounds. Commonly employed in Suzuki and Buchwald–Hartwig reactions to introduce the pyridine moiety into larger drug-like structures. Also utilized in agrochemical research for designing new active ingredients due to its electron-withdrawing properties and stability.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,600.00
inventory 5g
10-20 days ฿6,940.00
inventory 10g
10-20 days ฿13,860.00
inventory 25g
10-20 days ฿33,880.00

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4-Iodo-2-(trifluoromethyl)pyridine
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure allows for selective cross-coupling reactions, making it valuable in medicinal chemistry for building complex heterocyclic compounds. Commonly employed in Suzuki and Buchwald–Hartwig reactions to introduce the pyridine moiety into larger drug-like structures. Also utilized in agrochemical research for designing new active ingredients due to its ele
Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure allows for selective cross-coupling reactions, making it valuable in medicinal chemistry for building complex heterocyclic compounds. Commonly employed in Suzuki and Buchwald–Hartwig reactions to introduce the pyridine moiety into larger drug-like structures. Also utilized in agrochemical research for designing new active ingredients due to its electron-withdrawing properties and stability.
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