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

95%

Reagent Code: #148561
fingerprint
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.

Available Sizes & Pricing

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

Cart

No products

Subtotal: 0.00
Total 0.00 THB
tert-Butyl (6-chloro-3-iodopyridin-2-yl)carbamate
No image available

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.

Mechanism -
Appearance -
Longevity -
Strength -
Storage -
Shelf Life -
Allergen(s) -
Dosage (Range) -
Dosage (Per Day) -
Mix Method -
Heat Resistance -
Stable in pH range -
Solubility -
Product Types -
INCI -

Purchase History for

Loading purchase history...