Atomfair 2-Bromo-3-fluorobenzoic acid C7H4BrFO2

Description 2-Bromo-3-fluorobenzoic acid (CAS No. 132715-69-6) is a high-purity halogenated benzoic acid derivative with the molecular formula C7H4BrFO2. This compound is a valuable building block in organic synthesis, particularly in pharmaceutical and agrochemical research. The presence of both bromine and fluorine substituents on the aromatic ring enhances its reactivity, making it an ideal intermediate for cross-coupling reactions, nucleophilic substitutions, and other functionalization processes. Our product is rigorously tested to ensure ??98% purity (HPLC) and is supplied as a white to off-white crystalline powder. Suitable for use in medicinal chemistry, material science, and as a precursor for advanced chemical synthesis. Store…

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Description

Description

2-Bromo-3-fluorobenzoic acid (CAS No. 132715-69-6) is a high-purity halogenated benzoic acid derivative with the molecular formula C7H4BrFO2. This compound is a valuable building block in organic synthesis, particularly in pharmaceutical and agrochemical research. The presence of both bromine and fluorine substituents on the aromatic ring enhances its reactivity, making it an ideal intermediate for cross-coupling reactions, nucleophilic substitutions, and other functionalization processes. Our product is rigorously tested to ensure ??98% purity (HPLC) and is supplied as a white to off-white crystalline powder. Suitable for use in medicinal chemistry, material science, and as a precursor for advanced chemical synthesis. Store in a cool, dry place under inert conditions to maintain stability.

  • CAS No: 132715-69-6
  • Molecular Formula: C7H4BrFO2
  • Molecular Weight: 219.01
  • Exact Mass: 217.93787
  • Monoisotopic Mass: 217.93787
  • IUPAC Name: 2-bromo-3-fluorobenzoic acid
  • SMILES: C1=CC(=C(C(=C1)F)Br)C(=O)O
  • Synonyms: 2-Bromo-3-fluorobenzoic acid, 132715-69-6, DTXSID50307157, DTXCID80258284, 630-221-3

Application

2-Bromo-3-fluorobenzoic acid is widely used as a key intermediate in the synthesis of bioactive molecules, including pharmaceuticals and agrochemicals. Its halogenated aromatic structure facilitates Suzuki-Miyaura and Buchwald-Hartwig coupling reactions for constructing complex heterocycles. Researchers also employ it in the development of fluorinated liquid crystals and specialty polymers. The compound’s reactivity makes it valuable for introducing fluorine-containing motifs into target molecules.

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