tert-Butyl 4-(5-bromopyrazin-2-yl)piperazine-1-carboxylate

98%

Reagent Code: #140968
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CAS Number 622386-08-7

science Other reagents with same CAS 622386-08-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 343.23 g/mol
Formula C₁₃H₁₉BrN₄O₂
badge Registry Numbers
MDL Number MFCD11521572
inventory_2 Storage & Handling
Storage 2-8°C, 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 modification, making it valuable in medicinal chemistry for optimizing drug candidates. Commonly employed in cross-coupling reactions due to the presence of the bromo substituent, enabling the formation of carbon-heteroatom and carbon-carbon bonds. Also utilized in the preparation of library compounds for high-throughput screening in drug discovery programs.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿7,130.00
inventory 1g
10-20 days ฿32,680.00

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tert-Butyl 4-(5-bromopyrazin-2-yl)piperazine-1-carboxylate
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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 modification, making it valuable in medicinal chemistry for optimizing drug candidates. Commonly employed in cross-coupling reactions due to the presence of the bromo substituent, enabling the formation of carbon-heteroatom and carbon-carbon bonds. Also utilized in the preparation of library compounds for hig

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 modification, making it valuable in medicinal chemistry for optimizing drug candidates. Commonly employed in cross-coupling reactions due to the presence of the bromo substituent, enabling the formation of carbon-heteroatom and carbon-carbon bonds. Also utilized in the preparation of library compounds for high-throughput screening in drug discovery programs.

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