(3-Bromopyridin-2-yl)methanamine

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Reagent Code: #150046
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CAS Number 1053053-92-1

science Other reagents with same CAS 1053053-92-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 187.04 g/mol
Formula C₆H₇BrN₂
badge Registry Numbers
MDL Number MFCD13189050
inventory_2 Storage & Handling
Storage 2-8°C, avoid light, inert gas storage

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 constructing nitrogen-containing heterocyclic systems. Commonly employed in the preparation of agrochemicals and drug candidates due to its ability to participate in cross-coupling reactions and serve as a building block in multistep organic syntheses.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,650.00
inventory 250mg
10-20 days ฿7,440.00
inventory 1g
10-20 days ฿19,320.00

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(3-Bromopyridin-2-yl)methanamine
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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 constructing nitrogen-containing heterocyclic systems. Commonly employed in the preparation of agrochemicals and drug candidates due to its ability to participate in cross-coupling reactions and serve as a building block in multistep organic syntheses.
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 constructing nitrogen-containing heterocyclic systems. Commonly employed in the preparation of agrochemicals and drug candidates due to its ability to participate in cross-coupling reactions and serve as a building block in multistep organic syntheses.
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