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Structure of 1207175-60-7
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Methyl 3-amino-4-bromo-2-nitrobenzoate features a strategically positioned amino group enabling direct functionalization, while the bromine and nitro substituents provide orthogonal reactivity for cross-coupling and reduction sequences. This electron-deficient aryl scaffold supports efficient derivatization in synthetic routes to bioactive molecules and advanced intermediates.
Methyl 3-amino-4-bromo-2-nitrobenzoate serves as a versatile building block in medicinal chemistry and agrochemical synthesis, enabling sequential functionalization via orthogonal reactivity. The amino group facilitates nucleophilic substitution or coupling reactions, while the bromo and nitro functionalities support palladium-catalyzed cross-couplings and controlled reduction sequences. Its bench-stable nature and compatibility with standard purification methods make it well-suited for multi-step syntheses of complex heterocyclic scaffolds and API intermediates.
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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-H312-H332
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362+P364-P501
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Lot numbers can be found on the outside label of a product: