3-Bromo-6-methoxy-2-methyl-5-nitropyridine

95%

Reagent Code: #149096
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CAS Number 186413-76-3

science Other reagents with same CAS 186413-76-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 247.04608 g/mol
Formula C₇H₇BrN₂O₃
badge Registry Numbers
MDL Number MFCD11707229
inventory_2 Storage & Handling
Storage 2-8°C, dry, sealed

description Product Description

Used as an 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 medicinal chemistry for constructing complex heterocyclic compounds. 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 pyridine core and reactive bromine site.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,000.00
inventory 250mg
10-20 days ฿7,200.00

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3-Bromo-6-methoxy-2-methyl-5-nitropyridine
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Used as an 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 medicinal chemistry for constructing complex heterocyclic compounds. 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

Used as an 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 medicinal chemistry for constructing complex heterocyclic compounds. 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 pyridine core and reactive bromine site.

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