tert-Butyl (6-chloro-3-iodopyridin-2-yl)carbamate

95%

Reagent Code: #148561
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CAS Number 1622407-12-8

science Other reagents with same CAS 1622407-12-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 354.57 g/mol
Formula C₁₀H₁₂ClIN₂O₂
inventory_2 Storage & Handling
Storage 2-8°C, protected from light, stored in inert gas

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other biologically active molecules. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for constructing complex heterocyclic systems. Commonly employed in cross-coupling reactions due to the presence of iodine, enabling the formation of carbon-carbon bonds in drug discovery pathways. Also utilized in agrochemical research for designing novel active ingredients with improved stability and reactivity.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,870.00
inventory 250mg
10-20 days ฿5,050.00
inventory 1g
10-20 days ฿10,090.00

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tert-Butyl (6-chloro-3-iodopyridin-2-yl)carbamate
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other biologically active molecules. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for constructing complex heterocyclic systems. Commonly employed in cross-coupling reactions due to the presence of iodine, enabling the formation of carbon-carbon bonds in drug discovery pathways. Also utilized in agrochemical research for designin

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other biologically active molecules. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for constructing complex heterocyclic systems. Commonly employed in cross-coupling reactions due to the presence of iodine, enabling the formation of carbon-carbon bonds in drug discovery pathways. Also utilized in agrochemical research for designing novel active ingredients with improved stability and reactivity.

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