2-bromo-N-methylpyridin-3-amine

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Reagent Code: #215145
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CAS Number 872492-60-9

science Other reagents with same CAS 872492-60-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 187.0372 g/mol
Formula C₆H₇BrN₂
badge Registry Numbers
MDL Number MFCD07374348
thermostat Physical Properties
Boiling Point 282 °C
inventory_2 Storage & Handling
Density 1.581 g/cm3
Storage 2-8°C

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 structure allows for selective functionalization, making it valuable in medicinal chemistry for building complex molecules. Commonly employed in cross-coupling reactions such as Suzuki or Buchwald-Hartwig aminations to form carbon-nitrogen or carbon-carbon bonds. Also utilized in agrochemical research for designing novel pesticides and herbicides due to its ability to modulate biological activity in target organisms.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,840.00
inventory 250mg
10-20 days ฿6,400.00
inventory 1g
10-20 days ฿16,000.00
inventory 5g
10-20 days ฿57,600.00

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2-bromo-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 and other biologically active compounds. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for building complex molecules. Commonly employed in cross-coupling reactions such as Suzuki or Buchwald-Hartwig aminations to form carbon-nitrogen or carbon-carbon bonds. Also utilized in agrochemical research for designing novel pesticides and herbicide

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other biologically active compounds. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for building complex molecules. Commonly employed in cross-coupling reactions such as Suzuki or Buchwald-Hartwig aminations to form carbon-nitrogen or carbon-carbon bonds. Also utilized in agrochemical research for designing novel pesticides and herbicides due to its ability to modulate biological activity in target organisms.

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