6-Bromo-2-nitropyridin-3-ol

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Reagent Code: #151305
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CAS Number 443956-08-9

science Other reagents with same CAS 443956-08-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 218.99 g/mol
Formula C₅H₃BrN₂O₃
badge Registry Numbers
MDL Number MFCD09261204
thermostat Physical Properties
Boiling Point 413 °C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as an 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 Heck reactions to introduce aryl or vinyl groups. Also utilized in agrochemical research for designing novel pesticides and herbicides due to its electron-withdrawing nitro group and halogen substituent that enhance reactivity and binding properties.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿1,540.00
inventory 25g
10-20 days ฿6,400.00
inventory 100g
10-20 days ฿24,000.00

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6-Bromo-2-nitropyridin-3-ol
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Used as an 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 Heck reactions to introduce aryl or vinyl groups. Also utilized in agrochemical research for designing novel pesticides and herbicides due to its electron-

Used as an 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 Heck reactions to introduce aryl or vinyl groups. Also utilized in agrochemical research for designing novel pesticides and herbicides due to its electron-withdrawing nitro group and halogen substituent that enhance reactivity and binding properties.

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