5-Bromo-2-(dimethoxymethyl)-3-methoxypyridine

95%

Reagent Code: #149790
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CAS Number 1138443-86-3

science Other reagents with same CAS 1138443-86-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 262.1 g/mol
Formula C₉H₁₂BrNO₃
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MDL Number MFCD11857654
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key 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 pyridine-based compounds. Commonly employed in cross-coupling reactions such as Suzuki or Negishi couplings to introduce aryl or alkyl groups. Also utilized in agrochemical research for designing novel pesticides and herbicides due to its ability to enhance metabolic stability and binding affinity in target molecules.

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inventory 1g
10-20 days ฿67,360.00

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5-Bromo-2-(dimethoxymethyl)-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 bioactive molecules. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for constructing complex pyridine-based compounds. Commonly employed in cross-coupling reactions such as Suzuki or Negishi couplings to introduce aryl or alkyl groups. Also utilized in agrochemical research for designing novel pesticides and herbicides due to its a

Used as a key 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 pyridine-based compounds. Commonly employed in cross-coupling reactions such as Suzuki or Negishi couplings to introduce aryl or alkyl groups. Also utilized in agrochemical research for designing novel pesticides and herbicides due to its ability to enhance metabolic stability and binding affinity in target molecules.

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