Tert-Butyl 3-bromo-6-fluoropyridine-2-ca

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Reagent Code: #238570
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CAS Number 1430753-76-6

science Other reagents with same CAS 1430753-76-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 276.1022 g/mol
Formula C₁₀H₁₁BrFNO₂
badge Registry Numbers
MDL Number MFCD27988089
thermostat Physical Properties
Boiling Point 312.8±42.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.449±0.06 g/cm3(Predicted)
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 cross-coupling reactions, making it valuable in constructing complex heterocyclic systems found in drug candidates. Commonly employed in Suzuki and Negishi couplings to introduce the 6-fluoropyridin-2-yl moiety, which can enhance metabolic stability and binding affinity in target proteins. Also utilized in agrochemical research for designing novel pesticides with improved efficacy and selectivity.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿7,280.00
inventory 1g
10-20 days ฿13,730.00
inventory 5g
10-20 days ฿62,470.00
inventory 250mg
10-20 days ฿10,930.00

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Tert-Butyl 3-bromo-6-fluoropyridine-2-ca
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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 cross-coupling reactions, making it valuable in constructing complex heterocyclic systems found in drug candidates. Commonly employed in Suzuki and Negishi couplings to introduce the 6-fluoropyridin-2-yl moiety, which can enhance metabolic stability and binding affinity in target proteins. Also utilized in ag

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 cross-coupling reactions, making it valuable in constructing complex heterocyclic systems found in drug candidates. Commonly employed in Suzuki and Negishi couplings to introduce the 6-fluoropyridin-2-yl moiety, which can enhance metabolic stability and binding affinity in target proteins. Also utilized in agrochemical research for designing novel pesticides with improved efficacy and selectivity.

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