5-Bromo-2-ethoxy-3-methoxypyridine

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Reagent Code: #145068
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CAS Number 1241752-31-7

science Other reagents with same CAS 1241752-31-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 232.08 g/mol
Formula C₈H₁₀BrNO₂
badge Registry Numbers
MDL Number MFCD19688663
thermostat Physical Properties
Boiling Point 241.5±35.0°C
inventory_2 Storage & Handling
Storage Room temperature, dry

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 drug candidates targeting cancer and inflammatory diseases. Commonly employed in cross-coupling reactions such as Suzuki or Buchwald-Hartwig amination to build complex heterocyclic systems. Also utilized in agrochemical research for designing new pesticides and herbicides due to its stability and reactivity profile.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿3,000.00
inventory 250mg
10-20 days ฿9,600.00

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5-Bromo-2-ethoxy-3-methoxypyridine
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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 drug candidates targeting cancer and inflammatory diseases. Commonly employed in cross-coupling reactions such as Suzuki or Buchwald-Hartwig amination to build complex heterocyclic systems. Also utilized in agrochemical research for designing

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 drug candidates targeting cancer and inflammatory diseases. Commonly employed in cross-coupling reactions such as Suzuki or Buchwald-Hartwig amination to build complex heterocyclic systems. Also utilized in agrochemical research for designing new pesticides and herbicides due to its stability and reactivity profile.

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