5-Bromo-2-methylpyridin-3-amine

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Reagent Code: #151328
label
Alias 5-Bromo-2-methyl-3-aminopyridine; 3-amino-5-bromo-2-methylpyridine
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CAS Number 914358-73-9

science Other reagents with same CAS 914358-73-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 187.04 g/mol
Formula C₆H₇BrN₂
badge Registry Numbers
MDL Number MFCD09031418
thermostat Physical Properties
Melting Point 108-109 °C
inventory_2 Storage & Handling
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 and other bioactive molecules. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for creating compounds with high biological activity. Commonly employed in cross-coupling reactions such as Suzuki and Buchwald-Hartwig aminations to build complex heterocyclic systems found in drug candidates. Also utilized in agrochemical research for designing new pesticides and herbicides due to its stability and reactivity profile.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 10g
10-20 days ฿1,350.00
inventory 25g
10-20 days ฿3,350.00
inventory 100g
10-20 days ฿15,620.00

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5-Bromo-2-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 bioactive molecules. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for creating compounds with high biological activity. Commonly employed in cross-coupling reactions such as Suzuki and Buchwald-Hartwig aminations to build complex heterocyclic systems found in drug candidates. Also utilized in agrochemical research for designing n

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for creating compounds with high biological activity. Commonly employed in cross-coupling reactions such as Suzuki and Buchwald-Hartwig aminations to build complex heterocyclic systems found in drug candidates. Also utilized in agrochemical research for designing new pesticides and herbicides due to its stability and reactivity profile.

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