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Structure of 215949-57-8
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This brominated arylacetic acid features a para-bromo and meta-methyl substitution pattern on the phenyl ring, delivering enhanced electronic modulation and steric profile. The carboxylic acid functionality enables direct coupling or derivatization in synthetic routes. Bench-stable and moisture-tolerant, it serves as a key building block for pharmaceutical intermediates and functional materials.
2-(4-Bromo-3-methylphenyl)acetic acid serves as a versatile building block for the synthesis of biologically active molecules, particularly in medicinal chemistry and agrochemical research. Its structure features a brominated aromatic ring with a pendant acetic acid side chain, enabling diverse functionalization via palladium-catalyzed cross-coupling reactions. The compound exhibits good bench stability and facilitates straightforward purification, making it well-suited for use in multi-step synthetic sequences.
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Lot numbers can be found on the outside label of a product: