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Atomfair 4-Amino-6-bromo-3-chloro-5-fluoropicolinic acid C6H3BrClFN2O2

Description 4-Amino-6-bromo-3-chloro-5-fluoropicolinic acid (CAS No. 2413551-80-9) is a high-purity halogenated picolinic acid derivative with the molecular formula C6H3BrClFN2O2. This compound features a multifunctional pyridine core substituted with amino, bromo, chloro, fluoro, and carboxylic acid groups, making it a versatile building block for pharmaceutical and agrochemical research. With an IUPAC name of 4-amino-6-bromo-3-chloro-5-fluoropyridine-2-carboxylic acid , it is supplied as a crystalline solid with ??95% purity (HPLC). Ideal for cross-coupling reactions, heterocyclic synthesis, and structure-activity relationship (SAR) studies. Available in customizable quantities with batch-specific COA and NMR data.

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Description

Description

4-Amino-6-bromo-3-chloro-5-fluoropicolinic acid (CAS No. 2413551-80-9) is a high-purity halogenated picolinic acid derivative with the molecular formula C6H3BrClFN2O2. This compound features a multifunctional pyridine core substituted with amino, bromo, chloro, fluoro, and carboxylic acid groups, making it a versatile building block for pharmaceutical and agrochemical research. With an IUPAC name of 4-amino-6-bromo-3-chloro-5-fluoropyridine-2-carboxylic acid, it is supplied as a crystalline solid with ??95% purity (HPLC). Ideal for cross-coupling reactions, heterocyclic synthesis, and structure-activity relationship (SAR) studies. Available in customizable quantities with batch-specific COA and NMR data.

  • CAS No: 2413551-80-9
  • Molecular Formula: C6H3BrClFN2O2
  • Molecular Weight: 269.45
  • Exact Mass: 267.90505
  • Monoisotopic Mass: 267.90505
  • IUPAC Name: 4-amino-6-bromo-3-chloro-5-fluoropyridine-2-carboxylic acid
  • SMILES: C1(=C(C(=NC(=C1Cl)C(=O)O)Br)F)N
  • Synonyms: 4-Amino-6-bromo-3-chloro-5-fluoropicolinic acid, 2413551-80-9, SCHEMBL21806451, CS-0380709

Application

This polyhalogenated picolinic acid derivative serves as a key intermediate in the synthesis of bioactive molecules, particularly in the development of herbicides and pharmaceutical candidates. Its unique substitution pattern enables participation in Pd-catalyzed cross-coupling reactions for constructing complex heterocycles. Researchers utilize it as a scaffold for designing enzyme inhibitors targeting bacterial and plant pathogens.

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