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Structure of 573692-58-7
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Methyl 6-amino-3-bromo-2-methylbenzoate features a brominated aromatic core with complementary amino and ester functionalities, enabling direct incorporation into Suzuki-Miyaura cross-coupling and amide derivatization workflows. The para-amino group enhances electron density for reactive coupling, while the methyl substituent provides steric control. This bench-stable reagent supports efficient synthesis of functionalized heterocycles and bioactive scaffolds under standard conditions.
Methyl 6-amino-3-bromo-2-methylbenzoate serves as a versatile building block in medicinal chemistry and agrochemical synthesis, enabling palladium-catalyzed cross-coupling reactions due to its ortho-bromo and meta-amino functionalization. The methyl ester group provides a handle for selective derivatization, while the amino and bromo substituents offer orthogonal reactivity. Bench-stable and compatible with standard purification methods, it facilitates efficient access to substituted heterocycles and complex scaffolds in multi-step syntheses.
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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-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: