6,8-Dibromo-2-methyl-[1,2,4]triazolo[1,5-a]pyrazine

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Reagent Code: #133788
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CAS Number 1198475-31-8

science Other reagents with same CAS 1198475-31-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 291.93 g/mol
Formula C₆H₄Br₂N₄
badge Registry Numbers
MDL Number MFCD12406131
inventory_2 Storage & Handling
Density 2.40±0.1 g/cm3(Predicted)
Storage 2-8°C, Sealed, Inert Gas

description Product Description

Used in pharmaceutical research as a key intermediate in the synthesis of biologically active compounds, particularly kinase inhibitors. Shows potential in the development of anticancer agents due to its ability to modulate signaling pathways in cells. Also employed in agrochemical research for designing novel pesticides with improved efficacy and selectivity. Its bromine substituents allow for further functionalization via cross-coupling reactions, making it valuable in medicinal chemistry for building complex heterocyclic systems.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿10,210.00
inventory 250mg
10-20 days ฿17,340.00
inventory 1g
10-20 days ฿46,790.00

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6,8-Dibromo-2-methyl-[1,2,4]triazolo[1,5-a]pyrazine
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Used in pharmaceutical research as a key intermediate in the synthesis of biologically active compounds, particularly kinase inhibitors. Shows potential in the development of anticancer agents due to its ability to modulate signaling pathways in cells. Also employed in agrochemical research for designing novel pesticides with improved efficacy and selectivity. Its bromine substituents allow for further functionalization via cross-coupling reactions, making it valuable in medicinal chemistry for building

Used in pharmaceutical research as a key intermediate in the synthesis of biologically active compounds, particularly kinase inhibitors. Shows potential in the development of anticancer agents due to its ability to modulate signaling pathways in cells. Also employed in agrochemical research for designing novel pesticides with improved efficacy and selectivity. Its bromine substituents allow for further functionalization via cross-coupling reactions, making it valuable in medicinal chemistry for building complex heterocyclic systems.

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