5-Bromo-3-fluoropyridin-2(1H)-one

98%

Reagent Code: #145159
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CAS Number 156772-63-3

science Other reagents with same CAS 156772-63-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 191.99 g/mol
Formula C₅H₃BrFNO
badge Registry Numbers
MDL Number MFCD06659498
thermostat Physical Properties
Boiling Point 274.1°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other bioactive molecules targeting neurological and inflammatory disorders. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for constructing pyridine-based drug candidates. Commonly employed in cross-coupling reactions such as Suzuki-Miyaura and Buchwald-Hartwig aminations to build complex heterocyclic systems found in active pharmaceutical ingredients (APIs). Also utilized in agrochemical research for designing novel pesticides with improved selectivity and environmental profiles.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿3,410.00
inventory 10g
10-20 days ฿6,400.00
inventory 25g
10-20 days ฿15,460.00

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5-Bromo-3-fluoropyridin-2(1H)-one
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Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other bioactive molecules targeting neurological and inflammatory disorders. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for constructing pyridine-based drug candidates. Commonly employed in cross-coupling reactions such as Suzuki-Miyaura and Buchwald-Hartwig aminations to build complex heterocyclic systems found in active ph

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other bioactive molecules targeting neurological and inflammatory disorders. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for constructing pyridine-based drug candidates. Commonly employed in cross-coupling reactions such as Suzuki-Miyaura and Buchwald-Hartwig aminations to build complex heterocyclic systems found in active pharmaceutical ingredients (APIs). Also utilized in agrochemical research for designing novel pesticides with improved selectivity and environmental profiles.

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