3-Bromo-6-methylimidazo[1,2-a]pyrazine

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Reagent Code: #133806
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CAS Number 1276056-84-8

science Other reagents with same CAS 1276056-84-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 212.05 g/mol
Formula C₇H₆BrN₃
badge Registry Numbers
MDL Number MFCD18793415
thermostat Physical Properties
Melting Point 80-83 °C
inventory_2 Storage & Handling
Density 1.76±0.1 g/cm3(Predicted)
Storage 2-8°C, Sealed, Inert Gas

description Product Description

Used as a key intermediate in the synthesis of biologically active compounds, particularly in pharmaceuticals targeting central nervous system disorders and oncology. Its structure enables selective binding in kinase inhibitor development, making it valuable in drug discovery. Also employed in the preparation of fluorescent probes for biochemical assays due to its favorable photophysical properties. Commonly utilized in cross-coupling reactions to build complex heterocyclic systems in medicinal chemistry research.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿5,990.00

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3-Bromo-6-methylimidazo[1,2-a]pyrazine
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Used as a key intermediate in the synthesis of biologically active compounds, particularly in pharmaceuticals targeting central nervous system disorders and oncology. Its structure enables selective binding in kinase inhibitor development, making it valuable in drug discovery. Also employed in the preparation of fluorescent probes for biochemical assays due to its favorable photophysical properties. Commonly utilized in cross-coupling reactions to build complex heterocyclic systems in medicinal chemistry

Used as a key intermediate in the synthesis of biologically active compounds, particularly in pharmaceuticals targeting central nervous system disorders and oncology. Its structure enables selective binding in kinase inhibitor development, making it valuable in drug discovery. Also employed in the preparation of fluorescent probes for biochemical assays due to its favorable photophysical properties. Commonly utilized in cross-coupling reactions to build complex heterocyclic systems in medicinal chemistry research.

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