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Structure of 106976-24-3
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This brominated benzoic acid derivative features a para-substituted amino group and a methyl moiety, enabling direct integration into diverse synthetic scaffolds. The carboxylic acid functionality supports facile derivatization under standard coupling conditions, while the electron-withdrawing bromine enhances reactivity in cross-coupling processes. Bench-stable and moisture-tolerant, this compound serves as a key intermediate in pharmaceutical and agrochemical synthesis.
2-Amino-5-bromo-4-methylbenzoic acid serves as a versatile building block for the synthesis of heterocyclic scaffolds and bioactive molecules. Its well-defined functional group array—amino, bromo, methyl, and carboxylic acid—enables sequential transformations via Suzuki coupling, amidation, and electrophilic substitution. The compound exhibits good bench stability and facilitates straightforward purification, making it suitable for iterative medicinal chemistry campaigns and API intermediate 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 : H315-H319-H335
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Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: