2-Bromo-5-fluoronicotinaldehyde

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Reagent Code: #130000
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CAS Number 1227562-02-8

science Other reagents with same CAS 1227562-02-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 204 g/mol
Formula C₆H₃BrFNO
badge Registry Numbers
MDL Number MFCD16606507
inventory_2 Storage & Handling
Storage 2-8°C, Sealed, Inert Gas

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of nicotinamide-based drugs and kinase inhibitors. Its structure allows for selective functionalization in heterocyclic chemistry, making it valuable in creating bioactive molecules. Commonly employed in cross-coupling reactions such as Suzuki and Heck reactions to build complex aromatic systems. Also utilized in agrochemical research for designing novel pesticides with improved selectivity and efficacy. Its aldehyde group enables easy derivatization for use in Schiff base formation and other condensation reactions relevant to medicinal chemistry.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿9,540.00
inventory 250mg
10-20 days ฿15,900.00

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2-Bromo-5-fluoronicotinaldehyde
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of nicotinamide-based drugs and kinase inhibitors. Its structure allows for selective functionalization in heterocyclic chemistry, making it valuable in creating bioactive molecules. Commonly employed in cross-coupling reactions such as Suzuki and Heck reactions to build complex aromatic systems. Also utilized in agrochemical research for designing novel pesticides with improved selectivity and efficacy. Its a

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of nicotinamide-based drugs and kinase inhibitors. Its structure allows for selective functionalization in heterocyclic chemistry, making it valuable in creating bioactive molecules. Commonly employed in cross-coupling reactions such as Suzuki and Heck reactions to build complex aromatic systems. Also utilized in agrochemical research for designing novel pesticides with improved selectivity and efficacy. Its aldehyde group enables easy derivatization for use in Schiff base formation and other condensation reactions relevant to medicinal chemistry.

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