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Structure of 206548-14-3
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Methyl 2-amino-5-bromo-3-methylbenzoate features a brominated, electron-deficient aromatic core paired with a methyl ester and amino functionality. This combination enables direct incorporation into heterocyclic scaffolds and facilitates downstream derivatization in medicinal chemistry campaigns. The molecule exhibits enhanced stability under standard bench conditions.
Methyl 2-amino-5-bromo-3-methylbenzoate serves as a versatile building block in medicinal chemistry and agrochemical synthesis, enabling direct access to substituted benzimidazoles, benzoxazoles, and other heterocyclic scaffolds via standard coupling and cyclization protocols. The molecule’s ortho-amino and bromo groups facilitate sequential functionalization, while the methyl ester provides a handle for further derivatization. Bench-stable and readily purified by recrystallization or column chromatography, it supports scalable synthesis 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 : 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: