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Structure of 136285-65-9
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Ethyl 2-((tert-butoxycarbonyl)amino)-3-nitrobenzoate features a nitro group at the meta position relative to a protected amino function, enabling selective derivatization. The tert-butyl carbamate moiety provides stability and orthogonal deprotection capability, while the ester facilitates coupling reactions. This compound integrates readily into peptide synthesis and medicinal chemistry scaffolds under standard conditions.
Ethyl 2-((tert-butoxycarbonyl)amino)-3-nitrobenzoate serves as a versatile building block in medicinal chemistry, enabling the synthesis of substituted benzoic acid derivatives and heterocyclic scaffolds. The nitro group facilitates sequential transformations including reduction to an amine, while the Boc-protected amino function allows for orthogonal manipulation. Its bench-stable nature and compatibility with standard coupling and cyclization protocols make it ideal for multi-step syntheses requiring selective functionalization.
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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-P280-P302+P352
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Lot numbers can be found on the outside label of a product: