3-bromo-5-chloro-2-methoxypyridine

≥95%

Reagent Code: #144148
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CAS Number 102830-75-1

science Other reagents with same CAS 102830-75-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 222.47 g/mol
Formula C₆H₅BrClNO
badge Registry Numbers
MDL Number MFCD08059322
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of agrochemicals and active pharmaceutical ingredients (APIs). Its structure allows for selective functionalization, making it valuable in constructing complex pyridine-based molecules. Commonly employed in cross-coupling reactions such as Suzuki or Buchwald-Hartwig aminations to form carbon-carbon or carbon-nitrogen bonds. Also utilized in the production of herbicides and insecticides due to the bioactivity associated with halogenated pyridine derivatives. Its methoxy and halogen groups provide sites for further chemical modification, enabling tailored molecular design in drug discovery and crop protection chemistry.

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Test Parameter Specification
Purity 95-100
Refractive Index (N20/D) 1.56-1.57
Appearance SOLID

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿110.00
inventory 5g
10-20 days ฿300.00
inventory 25g
10-20 days ฿1,500.00
inventory 100g
10-20 days ฿5,890.00
inventory 500g
10-20 days ฿28,820.00

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3-bromo-5-chloro-2-methoxypyridine
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of agrochemicals and active pharmaceutical ingredients (APIs). Its structure allows for selective functionalization, making it valuable in constructing complex pyridine-based molecules. Commonly employed in cross-coupling reactions such as Suzuki or Buchwald-Hartwig aminations to form carbon-carbon or carbon-nitrogen bonds. Also utilized in the production of herbicides and insecticides due to the bioactivity a

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of agrochemicals and active pharmaceutical ingredients (APIs). Its structure allows for selective functionalization, making it valuable in constructing complex pyridine-based molecules. Commonly employed in cross-coupling reactions such as Suzuki or Buchwald-Hartwig aminations to form carbon-carbon or carbon-nitrogen bonds. Also utilized in the production of herbicides and insecticides due to the bioactivity associated with halogenated pyridine derivatives. Its methoxy and halogen groups provide sites for further chemical modification, enabling tailored molecular design in drug discovery and crop protection chemistry.

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