tert-Butyl (5-bromopyrazin-2-yl)carbamate

98%

Reagent Code: #145263
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CAS Number 914349-79-4

science Other reagents with same CAS 914349-79-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 274.11 g/mol
Formula C₉H₁₂BrN₃O₂
thermostat Physical Properties
Boiling Point 295.2°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as an intermediate in pharmaceutical synthesis, particularly in the development of kinase inhibitors and other biologically active compounds. Its structure allows for selective functionalization, making it valuable in constructing nitrogen-containing heterocycles. Commonly employed in cross-coupling reactions due to the presence of the bromo substituent, enabling the formation of C–C and C–N bonds. Also utilized in medicinal chemistry for the preparation of pyrazine-based drug candidates targeting cancer and inflammatory diseases.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿2,990.00
inventory 50mg
10-20 days ฿1,010.00
tert-Butyl (5-bromopyrazin-2-yl)carbamate
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Used as an intermediate in pharmaceutical synthesis, particularly in the development of kinase inhibitors and other biologically active compounds. Its structure allows for selective functionalization, making it valuable in constructing nitrogen-containing heterocycles. Commonly employed in cross-coupling reactions due to the presence of the bromo substituent, enabling the formation of C–C and C–N bonds. Also utilized in medicinal chemistry for the preparation of pyrazine-based drug candidates targeting c

Used as an intermediate in pharmaceutical synthesis, particularly in the development of kinase inhibitors and other biologically active compounds. Its structure allows for selective functionalization, making it valuable in constructing nitrogen-containing heterocycles. Commonly employed in cross-coupling reactions due to the presence of the bromo substituent, enabling the formation of C–C and C–N bonds. Also utilized in medicinal chemistry for the preparation of pyrazine-based drug candidates targeting cancer and inflammatory diseases.

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