5-bromo-2,3-difluoropyridine

98%

Reagent Code: #144162
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CAS Number 89402-44-8

science Other reagents with same CAS 89402-44-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 193.98 g/mol
Formula C₅H₂BrF₂N
badge Registry Numbers
MDL Number MFCD06659525
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of agrochemicals and active pharmaceutical ingredients (APIs). Its halogenated pyridine structure allows for selective cross-coupling reactions, making it valuable in building complex molecules for crop protection agents and medicinal compounds. Commonly employed in Suzuki and Buchwald–Hartwig reactions to introduce functionalized pyridine moieties. Also utilized in the preparation of kinase inhibitors and other biologically active compounds where fluorinated aromatics enhance metabolic stability and binding affinity.

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Test Parameter Specification
Appearance Colorless Liquid
Purity 97.5-100%
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿1,360.00
inventory 10g
10-20 days ฿2,640.00
inventory 100g
10-20 days ฿23,650.00
inventory 25g
10-20 days ฿6,130.00

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5-bromo-2,3-difluoropyridine
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of agrochemicals and active pharmaceutical ingredients (APIs). Its halogenated pyridine structure allows for selective cross-coupling reactions, making it valuable in building complex molecules for crop protection agents and medicinal compounds. Commonly employed in Suzuki and Buchwald–Hartwig reactions to introduce functionalized pyridine moieties. Also utilized in the preparation of kinase inhibitors and oth

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of agrochemicals and active pharmaceutical ingredients (APIs). Its halogenated pyridine structure allows for selective cross-coupling reactions, making it valuable in building complex molecules for crop protection agents and medicinal compounds. Commonly employed in Suzuki and Buchwald–Hartwig reactions to introduce functionalized pyridine moieties. Also utilized in the preparation of kinase inhibitors and other biologically active compounds where fluorinated aromatics enhance metabolic stability and binding affinity.

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