6-bromo-5-methylpyridin-3-ol

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Reagent Code: #143972
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CAS Number 1003711-43-0

science Other reagents with same CAS 1003711-43-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 188.02 g/mol
Formula C₆H₆BrNO
badge Registry Numbers
MDL Number MFCD09839267
thermostat Physical Properties
Boiling Point 377.2 °C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in the preparation of active pharmaceutical ingredients (APIs) due to its reactive bromo and hydroxyl functional groups, which allow for further chemical modifications. Commonly employed in cross-coupling reactions such as Suzuki or Buchwald-Hartwig aminations to construct complex heterocyclic systems found in bioactive molecules. Also utilized in agrochemical research for designing novel pesticides with improved selectivity and efficacy.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,460.00
inventory 5g
10-20 days ฿3,990.00
inventory 10g
10-20 days ฿6,900.00
inventory 25g
10-20 days ฿13,980.00

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6-bromo-5-methylpyridin-3-ol
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in the preparation of active pharmaceutical ingredients (APIs) due to its reactive bromo and hydroxyl functional groups, which allow for further chemical modifications. Commonly employed in cross-coupling reactions such as Suzuki or Buchwald-Hartwig aminations to construct complex heterocyclic systems found in bioactive molecules. Also ut

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in the preparation of active pharmaceutical ingredients (APIs) due to its reactive bromo and hydroxyl functional groups, which allow for further chemical modifications. Commonly employed in cross-coupling reactions such as Suzuki or Buchwald-Hartwig aminations to construct complex heterocyclic systems found in bioactive molecules. Also utilized in agrochemical research for designing novel pesticides with improved selectivity and efficacy.

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