Methyl 6-bromo-3-methoxypicolinate

98%

Reagent Code: #207254
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CAS Number 945954-94-9

science Other reagents with same CAS 945954-94-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 246.06 g/mol
Formula C₈H₈BrNO₃
badge Registry Numbers
MDL Number MFCD18257515
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the development of herbicides and fungicides. Its bromine and ester functionalities allow for further chemical modifications, making it valuable in constructing complex molecules. Commonly employed in cross-coupling reactions such as Suzuki or Heck reactions to form carbon-carbon bonds. Also utilized in the preparation of pyridine-based compounds with biological activity. Its methoxy and bromo substituents provide regioselective control during synthesis, enhancing its utility in fine chemical manufacturing.

Available Sizes & Pricing

Size Availability Unit Price Quantity
25mg
10-20 days ฿1,150.00
100mg
10-20 days ฿1,820.00
1g
10-20 days ฿8,840.00
Methyl 6-bromo-3-methoxypicolinate
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Used as a key intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the development of herbicides and fungicides. Its bromine and ester functionalities allow for further chemical modifications, making it valuable in constructing complex molecules. Commonly employed in cross-coupling reactions such as Suzuki or Heck reactions to form carbon-carbon bonds. Also utilized in the preparation of pyridine-based compounds with biological activity. Its methoxy and bromo substituents p

Used as a key intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the development of herbicides and fungicides. Its bromine and ester functionalities allow for further chemical modifications, making it valuable in constructing complex molecules. Commonly employed in cross-coupling reactions such as Suzuki or Heck reactions to form carbon-carbon bonds. Also utilized in the preparation of pyridine-based compounds with biological activity. Its methoxy and bromo substituents provide regioselective control during synthesis, enhancing its utility in fine chemical manufacturing.

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