2-Bromo-3-fluoropyrazine

95%

Reagent Code: #150842
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CAS Number 206278-27-5

science Other reagents with same CAS 206278-27-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 176.97 g/mol
Formula C₄H₂BrFN₂
badge Registry Numbers
MDL Number MFCD15144418
thermostat Physical Properties
Boiling Point 177.4±35.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.838±0.06 g/cm3(Predicted)
Storage Room temperature

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other biologically active compounds. 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 pyrazine-based scaffolds into drug candidates. Also utilized in agrochemical research for designing novel pesticides with improved efficacy and selectivity.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿6,840.00
inventory 250mg
10-20 days ฿10,350.00
inventory 1g
10-20 days ฿25,450.00

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2-Bromo-3-fluoropyrazine
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other biologically active compounds. 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 pyrazine-based scaffolds into drug candidates. Also utilized in agrochemical research for designing novel pesticides with

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other biologically active compounds. 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 pyrazine-based scaffolds into drug candidates. Also utilized in agrochemical research for designing novel pesticides with improved efficacy and selectivity.

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