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Structure of 147149-85-7
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6-Amino-2-bromo-3-methylbenzoic acid features a strategically positioned amino group and bromine atom on a methyl-substituted benzoic acid scaffold. This arrangement enables direct functionalization in cross-coupling reactions and facilitates incorporation into bioactive scaffolds. The carboxylic acid moiety supports conjugation via amide or ester linkages, while the electron-donating amino group enhances reactivity in electrophilic substitution. Bench-stable under standard conditions, this compound serves as a versatile intermediate for pharmaceutical and agrochemical synthesis.
6-Amino-2-bromo-3-methylbenzoic acid serves as a versatile building block for the synthesis of functionalized heterocycles and bioactive molecules. Its ortho-halogenated, amino-, and carboxylic acid functionalities enable sequential cross-coupling, amidation, and cyclization reactions. The molecule exhibits good bench stability and facilitates efficient purification via recrystallization, making it well-suited for scalable 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 : 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: