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Structure of 885519-13-1
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5-Bromo-1-chloro-2-methyl-3-nitrobenzene features a densely functionalized aromatic core with complementary halogen and nitro groups, enabling direct coupling in cross-coupling reactions. The methyl substituent provides steric bias, while the electron-deficient ring facilitates nucleophilic substitution under mild conditions. This compound serves as a key intermediate in the synthesis of advanced pharmaceuticals and agrochemicals.
5-Bromo-1-chloro-2-methyl-3-nitrobenzene serves as a versatile building block in medicinal chemistry and agrochemical synthesis, enabling selective cross-coupling reactions via its bromo and chloro substituents. The nitro group facilitates downstream functionalization, while the methyl group provides steric and electronic modulation. This compound exhibits excellent bench stability, ease of purification, and compatibility with standard Pd-catalyzed coupling protocols, making it well-suited for multi-step synthetic sequences.
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Lot numbers can be found on the outside label of a product: