tert-Butyl 4-amino-5-bromopyridine-2-carboxylate

96%

Reagent Code: #150328
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CAS Number 868171-70-4

science Other reagents with same CAS 868171-70-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 273.13 g/mol
Formula C₁₀H₁₃BrN₂O₂
badge Registry Numbers
MDL Number MFCD14706240
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used as a key 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 nitrogen-containing heterocycles. Commonly employed in cross-coupling reactions due to the presence of the bromine moiety, enabling the formation of carbon-carbon bonds in drug discovery pathways. Also utilized in the preparation of agrochemicals and functional materials where pyridine derivatives are required.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿8,360.00
inventory 250mg
10-20 days ฿13,780.00
inventory 1g
10-20 days ฿27,330.00

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tert-Butyl 4-amino-5-bromopyridine-2-carboxylate
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Used as a key 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 nitrogen-containing heterocycles. Commonly employed in cross-coupling reactions due to the presence of the bromine moiety, enabling the formation of carbon-carbon bonds in drug discovery pathways. Also utilized in the preparation

Used as a key 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 nitrogen-containing heterocycles. Commonly employed in cross-coupling reactions due to the presence of the bromine moiety, enabling the formation of carbon-carbon bonds in drug discovery pathways. Also utilized in the preparation of agrochemicals and functional materials where pyridine derivatives are required.

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