Methyl 6-bromo-2-methoxynicotinate

≥98%

Reagent Code: #208852
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CAS Number 1009735-24-3

science Other reagents with same CAS 1009735-24-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 246.06 g/mol
Formula C₈H₈BrNO₃
badge Registry Numbers
MDL Number MFCD18257518
thermostat Physical Properties
Boiling Point 296.5±35.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, stored in inert gas

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other biologically active compounds. Its structure allows for selective functionalization, making it valuable in building complex heterocyclic systems found in drug candidates. Commonly employed in cross-coupling reactions such as Suzuki or Heck reactions to introduce aryl or vinyl groups. Also utilized in agrochemical research for designing novel pesticides and herbicides due to its ability to modulate biological activity in target organisms.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,400.00
inventory 250mg
10-20 days ฿3,330.00
inventory 5g
10-20 days ฿28,800.00
inventory 25g
10-20 days ฿104,000.00
inventory 1g
10-20 days ฿9,600.00

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Methyl 6-bromo-2-methoxynicotinate
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other biologically active compounds. Its structure allows for selective functionalization, making it valuable in building complex heterocyclic systems found in drug candidates. Commonly employed in cross-coupling reactions such as Suzuki or Heck reactions to introduce aryl or vinyl 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 biologically active compounds. Its structure allows for selective functionalization, making it valuable in building complex heterocyclic systems found in drug candidates. Commonly employed in cross-coupling reactions such as Suzuki or Heck reactions to introduce aryl or vinyl groups. Also utilized in agrochemical research for designing novel pesticides and herbicides due to its ability to modulate biological activity in target organisms.

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