Methyl 6-bromo-5-fluoropyridine-2-carboxylate

≥95%

Reagent Code: #205647
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CAS Number 1210419-26-3

science Other reagents with same CAS 1210419-26-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 234.02 g/mol
Formula C₇H₅BrFNO₂
badge Registry Numbers
MDL Number MFCD14698111
inventory_2 Storage & Handling
Storage Room temperature

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 heterocyclic compounds. Commonly employed in cross-coupling reactions such as Suzuki or Buchwald-Hartwig aminations to introduce aryl or amino 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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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿2,320.00
inventory 5g
10-20 days ฿8,950.00
inventory 10g
10-20 days ฿17,880.00
inventory 25g
10-20 days ฿40,070.00
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Methyl 6-bromo-5-fluoropyridine-2-carboxylate
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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 heterocyclic compounds. Commonly employed in cross-coupling reactions such as Suzuki or Buchwald-Hartwig aminations to introduce aryl or amino groups. Also utilized in agrochemical research for designing novel pesticides and herbicides due

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 heterocyclic compounds. Commonly employed in cross-coupling reactions such as Suzuki or Buchwald-Hartwig aminations to introduce aryl or amino 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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