5-Bromo-4-chloropyridin-3-amine

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Reagent Code: #146230
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CAS Number 89283-92-1

science Other reagents with same CAS 89283-92-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 207.46 g/mol
Formula C₅H₄BrClN₂
badge Registry Numbers
MDL Number MFCD12828485
inventory_2 Storage & Handling
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 creating targeted therapies. It is also employed in agrochemical research for designing novel pesticides and herbicides due to its ability to enhance binding affinity with biological targets. The compound's halogenated pyridine core supports cross-coupling reactions, enabling efficient construction of complex molecules in drug discovery and process chemistry.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿600.00
inventory 1g
10-20 days ฿1,900.00
inventory 5g
10-20 days ฿7,800.00

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5-Bromo-4-chloropyridin-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 creating targeted therapies. It is also employed in agrochemical research for designing novel pesticides and herbicides due to its ability to enhance binding affinity with biological targets. The compound's halogenated pyridine core supports cross-cou

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 creating targeted therapies. It is also employed in agrochemical research for designing novel pesticides and herbicides due to its ability to enhance binding affinity with biological targets. The compound's halogenated pyridine core supports cross-coupling reactions, enabling efficient construction of complex molecules in drug discovery and process chemistry.

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