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Structure of 20776-67-4
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2-Amino-5-chloro-3-methylbenzoic acid features a trifunctional aromatic core with electron-donating amine and methyl groups paired with an electron-withdrawing chlorine, enabling tailored reactivity in pharmaceutical intermediates. The carboxylic acid moiety facilitates direct coupling or derivatization under standard conditions. This scaffold exhibits excellent stability and solubility in common organic solvents, supporting seamless integration into multi-step synthesis workflows.
2-Amino-5-chloro-3-methylbenzoic acid serves as a versatile building block in medicinal chemistry, enabling the synthesis of substituted benzimidazoles and other heterocyclic scaffolds. Its ortho-amino and carboxylic acid functionalities facilitate efficient coupling reactions and cyclizations, while the chloro and methyl groups provide defined electronic and steric profiles for targeted derivatization. The compound exhibits good bench stability and is compatible with standard purification methods.
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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 : H317
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Precautionary Statements : P261-P272-P280-P302+P352-P363-P501
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Lot numbers can be found on the outside label of a product: