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Structure of 849792-91-2
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Methyl 2-amino-4-((tert-butoxycarbonyl)amino)benzoate features a strategically positioned tert-butoxycarbonyl group that enables selective deprotection, while the methyl ester and amino functionalities offer orthogonal reactivity. This compound serves as a key intermediate in the synthesis of substituted benzamides and bioactive heterocycles under standard conditions.
Methyl 2-amino-4-((tert-butoxycarbonyl)amino)benzoate serves as a versatile building block in medicinal chemistry, enabling the synthesis of substituted benzimidazoles and other heterocyclic scaffolds. The ortho-amino and protected amine functionalities offer orthogonal reactivity for sequential functionalization. Its bench-stable tert-butyl carbamate group facilitates selective deprotection, while the methyl ester permits controlled hydrolysis or coupling reactions. This compound functions reliably in standard peptide-like coupling protocols and supports modular construction of complex nitrogen-containing architectures.
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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: