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Structure of 1261895-84-4
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2-Bromo-4-chloro-6-methoxyaniline features a tri-substituted aniline core with complementary halogen and methoxy functionalities, enabling direct coupling in cross-coupling reactions. The electron-donating methoxy group enhances nucleophilicity at the ortho position, while the bromo and chloro substituents provide orthogonal reactivity for sequential functionalization. This compound serves as a high-precision intermediate in the synthesis of complex heterocycles and bioactive molecules.
2-Bromo-4-chloro-6-methoxyaniline serves as a versatile building block in medicinal chemistry and agrochemical synthesis, enabling efficient access to substituted heterocycles via Pd-catalyzed cross-coupling reactions. Its ortho-bromo functionality facilitates C–C bond formation under standard Suzuki, Stille, or Negishi conditions, while the meta-chloro and para-methoxy groups provide orthogonal reactivity and enhanced solubility. The compound exhibits excellent bench stability and is readily purified by crystallization, supporting reliable scale-up in process development workflows.
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GHS Pictogram :
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H315-H319
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Precautionary Statements : P264-P280-P302+P352-P362
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Lot numbers can be found on the outside label of a product: