Ethyl 5-bromo-3-methylpicolinate

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Reagent Code: #120163
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CAS Number 794592-13-5

science Other reagents with same CAS 794592-13-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 244.09 g/mol
Formula C₉H₁₀BrNO₂
badge Registry Numbers
MDL Number MFCD15523779
inventory_2 Storage & Handling
Storage room temperature, stored under inert gas

description Product Description

Ethyl 5-bromo-3-methylpicolinate is primarily utilized in organic synthesis as a key intermediate for the development of more complex chemical compounds. Its structure makes it valuable in the synthesis of pharmaceuticals, particularly in the creation of active pharmaceutical ingredients (APIs) that target specific biological pathways. The bromine atom in the molecule allows for further functionalization through cross-coupling reactions, such as Suzuki or Heck reactions, which are essential in medicinal chemistry for building diverse molecular architectures. Additionally, it serves as a precursor in agrochemical research for designing novel pesticides or herbicides. Its ester group also provides versatility, enabling hydrolysis or transesterification to modify the compound for specific applications. Overall, it plays a significant role in advancing drug discovery and agricultural innovation.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿3,380.00
inventory 1g
10-20 days ฿730.00
inventory 10g
10-20 days ฿6,180.00
inventory 25g
10-20 days ฿12,700.00

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Ethyl 5-bromo-3-methylpicolinate
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Ethyl 5-bromo-3-methylpicolinate is primarily utilized in organic synthesis as a key intermediate for the development of more complex chemical compounds. Its structure makes it valuable in the synthesis of pharmaceuticals, particularly in the creation of active pharmaceutical ingredients (APIs) that target specific biological pathways. The bromine atom in the molecule allows for further functionalization through cross-coupling reactions, such as Suzuki or Heck reactions, which are essential in medicinal

Ethyl 5-bromo-3-methylpicolinate is primarily utilized in organic synthesis as a key intermediate for the development of more complex chemical compounds. Its structure makes it valuable in the synthesis of pharmaceuticals, particularly in the creation of active pharmaceutical ingredients (APIs) that target specific biological pathways. The bromine atom in the molecule allows for further functionalization through cross-coupling reactions, such as Suzuki or Heck reactions, which are essential in medicinal chemistry for building diverse molecular architectures. Additionally, it serves as a precursor in agrochemical research for designing novel pesticides or herbicides. Its ester group also provides versatility, enabling hydrolysis or transesterification to modify the compound for specific applications. Overall, it plays a significant role in advancing drug discovery and agricultural innovation.

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