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Structure of 2486-70-6
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4-Amino-3-methylbenzoic acid features a strategically positioned amino group and methyl substituent on the aromatic ring, enabling precise tuning of electronic properties and solubility. This ortho-substituted benzoic acid derivative serves as a key intermediate in the synthesis of bioactive compounds and functional materials, offering enhanced reactivity in coupling and derivatization processes under standard conditions.
4-Amino-3-methylbenzoic acid serves as a versatile building block in medicinal chemistry and agrochemical synthesis, enabling access to diverse heterocyclic scaffolds through standard coupling and cyclization protocols. Its ortho-substituted aryl functionality provides enhanced metabolic stability and tunable solubility, while the amino and carboxylic acid groups offer orthogonal reactivity for peptide coupling, amide formation, and derivatization. Bench-stable and readily purified by recrystallization, it functions reliably in multi-step syntheses requiring functional group compatibility and structural precision.
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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 : P233-P261-P264-P271-P272-P280-P285-P302+P352-P304+P340-P405-P501
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Lot numbers can be found on the outside label of a product: