4-Bromo-3-methylpicolinic acid

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Reagent Code: #148786
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CAS Number 1211526-84-9

science Other reagents with same CAS 1211526-84-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 216.03 g/mol
Formula C₇H₆BrNO₂
badge Registry Numbers
MDL Number MFCD18257506
inventory_2 Storage & Handling
Storage 2-8°C, stored in inert gas

description Product Description

Used in the synthesis of pharmaceutical intermediates, particularly in the development of kinase inhibitors and other bioactive molecules. Its halogenated structure makes it suitable for cross-coupling reactions, such as Suzuki or Buchwald-Hartwig reactions, enabling the construction of complex aromatic systems in drug discovery. Also employed as a building block in agrochemicals and functional materials where substituted pyridine derivatives are required. The carboxylic acid group allows for easy derivatization into amides, esters, or other functional groups to tune solubility and reactivity in synthetic pathways.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,810.00
inventory 250mg
10-20 days ฿4,700.00

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4-Bromo-3-methylpicolinic acid
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Used in the synthesis of pharmaceutical intermediates, particularly in the development of kinase inhibitors and other bioactive molecules. Its halogenated structure makes it suitable for cross-coupling reactions, such as Suzuki or Buchwald-Hartwig reactions, enabling the construction of complex aromatic systems in drug discovery. Also employed as a building block in agrochemicals and functional materials where substituted pyridine derivatives are required. The carboxylic acid group allows for easy deriva

Used in the synthesis of pharmaceutical intermediates, particularly in the development of kinase inhibitors and other bioactive molecules. Its halogenated structure makes it suitable for cross-coupling reactions, such as Suzuki or Buchwald-Hartwig reactions, enabling the construction of complex aromatic systems in drug discovery. Also employed as a building block in agrochemicals and functional materials where substituted pyridine derivatives are required. The carboxylic acid group allows for easy derivatization into amides, esters, or other functional groups to tune solubility and reactivity in synthetic pathways.

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