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Structure of 66315-16-0
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Methyl 3-amino-4-(methylamino)benzoate features a dual amine handle—primary amino and N-methylamino—positioned ortho to the ester group, enabling selective derivatization. This arrangement supports efficient coupling reactions in peptide synthesis and bioconjugation workflows. The molecule exhibits enhanced solubility in polar organic solvents and stability under standard bench conditions.
Methyl 3-amino-4-(methylamino)benzoate serves as a versatile building block in medicinal chemistry, enabling the synthesis of substituted benzimidazoles and other heterocyclic scaffolds via condensation and cyclization reactions. The ortho-amino and methylamino groups provide complementary reactivity for sequential functionalization, while the ester moiety allows for controlled derivatization. Bench-stable and readily purified by crystallization, it facilitates efficient access to complex molecular architectures in API development workflows.
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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: