5-Bromo-3-iodo-1-methylpyridin-2(1H)-one

98%

Reagent Code: #141478
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CAS Number 1643367-68-3

science Other reagents with same CAS 1643367-68-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 313.92 g/mol
Formula C₆H₅BrINO
inventory_2 Storage & Handling
Storage 2-8 °C, sealed, dry, protected from light

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. Its halogenated structure allows for selective cross-coupling reactions, making it valuable in medicinal chemistry for building complex heterocyclic systems. Commonly employed in Suzuki and Buchwald–Hartwig reactions to introduce functionalized pyridine moieties into drug candidates. Also utilized in agrochemical research for designing novel active ingredients with improved metabolic stability.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿10,820.00
inventory 250mg
10-20 days ฿15,500.00
inventory 500mg
10-20 days ฿28,830.00
inventory 1g
10-20 days ฿37,800.00
inventory 5g
10-20 days ฿132,300.00
inventory 25g
10-20 days ฿463,050.00

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5-Bromo-3-iodo-1-methylpyridin-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. Its halogenated structure allows for selective cross-coupling reactions, making it valuable in medicinal chemistry for building complex heterocyclic systems. Commonly employed in Suzuki and Buchwald–Hartwig reactions to introduce functionalized pyridine moieties into drug candidates. Also utilized in agrochemical research for designing novel active i

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other bioactive molecules. Its halogenated structure allows for selective cross-coupling reactions, making it valuable in medicinal chemistry for building complex heterocyclic systems. Commonly employed in Suzuki and Buchwald–Hartwig reactions to introduce functionalized pyridine moieties into drug candidates. Also utilized in agrochemical research for designing novel active ingredients with improved metabolic stability.

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