2-bromo-6-methyl-4-nitro-pyridine 1-oxide

95%

Reagent Code: #142420
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CAS Number 60323-99-1

science Other reagents with same CAS 60323-99-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 233.02 g/mol
Formula C₆H₅BrN₂O₃
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used as an 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 building complex heterocyclic systems. Commonly employed in cross-coupling reactions such as Suzuki or Buchwald-Hartwig aminations to introduce aryl or amino groups. Also utilized in agrochemical research for designing novel pesticides and herbicides due to its electron-deficient ring system that enhances binding to biological targets.

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Test Parameter Specification
Appearance Yellow Solid
Purity (%) 94.5-100%
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿11,160.00
inventory 1g
10-20 days ฿33,480.00
inventory 100mg
10-20 days ฿5,080.00

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2-bromo-6-methyl-4-nitro-pyridine 1-oxide
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Used as an 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 building complex heterocyclic systems. Commonly employed in cross-coupling reactions such as Suzuki or Buchwald-Hartwig aminations to introduce aryl or amino groups. Also utilized in agrochemical research for designing novel pesticides and herbicides due

Used as an 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 building complex heterocyclic systems. Commonly employed in cross-coupling reactions such as Suzuki or Buchwald-Hartwig aminations to introduce aryl or amino groups. Also utilized in agrochemical research for designing novel pesticides and herbicides due to its electron-deficient ring system that enhances binding to biological targets.

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