3-Amino-5-bromo-2-methoxypyridine

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Reagent Code: #135215
label
Alias 5-Bromo-2-methoxypyridine
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CAS Number 884495-39-0

science Other reagents with same CAS 884495-39-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 203.04 g/mol
Formula C₆H₇BrN₂O
thermostat Physical Properties
Boiling Point 266.5ºC at 760 mmHg
inventory_2 Storage & Handling
Density 1.65g/cm3
Storage Room temperature

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 creating compounds with specific biological activity. Commonly employed in research and development for agrochemicals and medicinal chemistry due to its ability to participate in cross-coupling reactions and serve as a building block in heterocyclic synthesis.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿162.00
inventory 5g
10-20 days ฿440.00
inventory 25g
10-20 days ฿1,260.00
inventory 100g
10-20 days ฿8,300.00

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3-Amino-5-bromo-2-methoxypyridine
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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 creating compounds with specific biological activity. Commonly employed in research and development for agrochemicals and medicinal chemistry due to its ability to participate in cross-coupling reactions and serve as a building block in heterocyclic synthesis.

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 creating compounds with specific biological activity. Commonly employed in research and development for agrochemicals and medicinal chemistry due to its ability to participate in cross-coupling reactions and serve as a building block in heterocyclic synthesis.

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