5-Bromo-4-chloro-2-methylpyridine 1-oxide

95%

Reagent Code: #141118
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CAS Number 103971-43-3

science Other reagents with same CAS 103971-43-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 222.46 g/mol
Formula C₆H₅NOClBr
badge Registry Numbers
MDL Number MFCD25954706
thermostat Physical Properties
Boiling Point 390.8±37.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.71±0.1 g/cm3(Predicted)
Storage 2-8°C, Inert Gas

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 drug candidates. Also employed in agrochemical research for designing novel pesticides and herbicides due to its ability to enhance molecular binding and stability. The N-oxide group facilitates specific reaction pathways, enabling efficient coupling reactions in heterocyclic chemistry.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿10,840.00
inventory 250mg
10-20 days ฿18,410.00
inventory 1g
10-20 days ฿49,690.00

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5-Bromo-4-chloro-2-methylpyridine 1-oxide
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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 drug candidates. Also employed in agrochemical research for designing novel pesticides and herbicides due to its ability to enhance molecular binding and stability. The N-oxide group facilitates specific reaction pathways, enabling effi
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 drug candidates. Also employed in agrochemical research for designing novel pesticides and herbicides due to its ability to enhance molecular binding and stability. The N-oxide group facilitates specific reaction pathways, enabling efficient coupling reactions in heterocyclic chemistry.
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