2,6-Dibromo-N-methylpyridin-3-amine

95%

Reagent Code: #215628
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CAS Number 84539-50-4

science Other reagents with same CAS 84539-50-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 265.93 g/mol
Formula C₆H₆Br₂N₂
badge Registry Numbers
MDL Number MFCD00234176
thermostat Physical Properties
Melting Point 69 °C(Solv: ethanol (64-17-5); water (7732-18-5))
Boiling Point 327.8±42.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.977±0.06 g/cm3(Predicted)
Storage Room temperature, light-proof, inert gas

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in medicinal chemistry due to its halogenated pyridine structure, which allows for further functionalization through cross-coupling reactions. Commonly employed in the preparation of biologically active compounds targeting neurological disorders and inflammatory diseases. 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 ฿7,560.00
inventory 250mg
10-20 days ฿12,770.00
inventory 1g
10-20 days ฿34,420.00

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2,6-Dibromo-N-methylpyridin-3-amine
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in medicinal chemistry due to its halogenated pyridine structure, which allows for further functionalization through cross-coupling reactions. Commonly employed in the preparation of biologically active compounds targeting neurological disorders and inflammatory diseases. Also utilized in agrochemical research for designing novel pesticides
Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in medicinal chemistry due to its halogenated pyridine structure, which allows for further functionalization through cross-coupling reactions. Commonly employed in the preparation of biologically active compounds targeting neurological disorders and inflammatory diseases. Also utilized in agrochemical research for designing novel pesticides with improved efficacy and selectivity.
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