3-Bromo-2-fluoropyridin-4-amine

95%

Reagent Code: #151207
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CAS Number 1364917-17-8

science Other reagents with same CAS 1364917-17-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 191.00 g/mol
Formula C₅H₄BrFN₂
badge Registry Numbers
MDL Number MFCD22199520
thermostat Physical Properties
Boiling Point 290.5±35.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.813±0.06 g/cm3(Predicted)
Storage Room temperature, light-proof storage, inert atmosphere

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 creating analogs with improved potency and selectivity. Commonly employed in cross-coupling reactions to form carbon-nitrogen or carbon-carbon bonds, it contributes to the construction of complex heterocyclic systems found in drug candidates. Also utilized in agrochemical research for designing novel pesticides and herbicides due to its ability to enhance metabolic stability and bioavailability in target compounds.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿7,050.00
inventory 1g
10-20 days ฿15,010.00

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3-Bromo-2-fluoropyridin-4-amine
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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 creating analogs with improved potency and selectivity. Commonly employed in cross-coupling reactions to form carbon-nitrogen or carbon-carbon bonds, it contributes to the construction of complex heterocyclic systems found in drug candidates.

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 creating analogs with improved potency and selectivity. Commonly employed in cross-coupling reactions to form carbon-nitrogen or carbon-carbon bonds, it contributes to the construction of complex heterocyclic systems found in drug candidates. Also utilized in agrochemical research for designing novel pesticides and herbicides due to its ability to enhance metabolic stability and bioavailability in target compounds.

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