5-Chloro-4-iodo-2-(trifluoromethyl)pyridine

98%

Reagent Code: #160703
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CAS Number 823221-95-0

science Other reagents with same CAS 823221-95-0

blur_circular Chemical Specifications

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Weight 307.44 g/mol
Formula C₆H₂ClF₃IN
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of herbicides and fungicides. Its halogen substituents enable selective cross-coupling reactions, making it valuable in medicinal chemistry for building complex molecules. Commonly employed in Suzuki and Buchwald–Hartwig reactions to introduce pyridine-based scaffolds into active compounds. Also utilized in the preparation of kinase inhibitors and other biologically active agents due to its electron-withdrawing properties and structural stability.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿850.00
inventory 100mg
10-20 days ฿1,720.00
inventory 250mg
10-20 days ฿3,440.00
inventory 1g
10-20 days ฿11,000.00
inventory 5g
10-20 days ฿43,990.00

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5-Chloro-4-iodo-2-(trifluoromethyl)pyridine
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Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of herbicides and fungicides. Its halogen substituents enable selective cross-coupling reactions, making it valuable in medicinal chemistry for building complex molecules. Commonly employed in Suzuki and Buchwald–Hartwig reactions to introduce pyridine-based scaffolds into active compounds. Also utilized in the preparation of kinase inhibitors and other biologically active agents due to its e

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of herbicides and fungicides. Its halogen substituents enable selective cross-coupling reactions, making it valuable in medicinal chemistry for building complex molecules. Commonly employed in Suzuki and Buchwald–Hartwig reactions to introduce pyridine-based scaffolds into active compounds. Also utilized in the preparation of kinase inhibitors and other biologically active agents due to its electron-withdrawing properties and structural stability.

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