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

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Weight 246.06 g/mol
Formula C₈H₈BrNO₃
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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.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿1,150.00
inventory 100mg
10-20 days ฿1,820.00
inventory 1g
10-20 days ฿8,840.00

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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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