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Structure of 256935-85-0
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Methyl 4-amino-2-chloro-5-iodobenzoate features a trifunctional aromatic core with orthogonal reactivity, enabling selective coupling in late-stage diversification. The electron-donating amino group enhances nucleophilicity at C4, while the chloro and iodo substituents provide complementary handles for palladium-catalyzed cross-coupling. This combination delivers precise control over molecular architecture in synthetic sequences.
Methyl 4-amino-2-chloro-5-iodobenzoate serves as a versatile building block for the synthesis of functionalized aromatic scaffolds. The molecule combines ortho-halogen (Cl, I) and amino functionalities, enabling sequential cross-coupling reactions such as Suzuki-Miyaura or Buchwald-Hartwig transformations. Its methyl ester group provides a handle for further derivatization, while the amino moiety offers nucleophilic reactivity. Bench-stable and readily purified by crystallization, it facilitates efficient access to complex heterocyclic systems and medicinally relevant frameworks in medicinal chemistry and process development.
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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 : H302-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: