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Structure of 52130-17-3
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3-Amino-2-methylbenzoic acid features a strategically positioned amino group adjacent to a carboxylic acid, enabling direct conjugation in peptide mimetics and bioactive scaffolds. The methyl substituent enhances lipophilicity and metabolic stability, while the ortho-amino functionality facilitates metal chelation and coordination chemistry. This compound serves as a key building block for pharmaceutical intermediates and functional materials requiring precise electronic tuning.
3-Amino-2-methylbenzoic acid serves as a versatile building block in medicinal chemistry, enabling the synthesis of bioactive heterocycles and pharmaceutical intermediates. Its ortho-substituted structure provides enhanced stability and facilitates selective functionalization, while the carboxylic acid and primary amine groups offer complementary handles for coupling reactions, derivatization, and salt formation. The molecule exhibits good bench stability and compatibility with standard purification techniques, making it well-suited for iterative synthetic workflows in API 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-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: