3-Bromo-6-methylpyridazine

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Reagent Code: #145211
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CAS Number 65202-58-6

science Other reagents with same CAS 65202-58-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 173.01 g/mol
Formula C₅H₅BrN₂
thermostat Physical Properties
Boiling Point 285°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used primarily as an intermediate in the synthesis of pharmaceuticals and agrochemicals. Its structure allows for selective functionalization in heterocyclic compounds, making it valuable in the development of bioactive molecules. Commonly employed in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig, to build complex pyridazine derivatives. Also explored in medicinal chemistry for the design of kinase inhibitors and other targeted therapies due to the pyridazine core's favorable binding properties.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿940.00
inventory 5g
10-20 days ฿4,680.00
inventory 10g
10-20 days ฿9,140.00
inventory 25g
10-20 days ฿19,850.00

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3-Bromo-6-methylpyridazine
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Used primarily as an intermediate in the synthesis of pharmaceuticals and agrochemicals. Its structure allows for selective functionalization in heterocyclic compounds, making it valuable in the development of bioactive molecules. Commonly employed in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig, to build complex pyridazine derivatives. Also explored in medicinal chemistry for the design of kinase inhibitors and other targeted therapies due to the pyridazine core's favorable binding prope

Used primarily as an intermediate in the synthesis of pharmaceuticals and agrochemicals. Its structure allows for selective functionalization in heterocyclic compounds, making it valuable in the development of bioactive molecules. Commonly employed in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig, to build complex pyridazine derivatives. Also explored in medicinal chemistry for the design of kinase inhibitors and other targeted therapies due to the pyridazine core's favorable binding properties.

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