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Structure of 208772-41-2
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This protected indoline derivative features a tert-butoxycarbonyl group at the nitrogen and a carboxylic acid at the 6-position, enabling selective functionalization in peptide coupling and heterocyclic synthesis. The Boc protection ensures stability under standard reaction conditions while allowing facile deprotection with mild acid.
1-(tert-Butoxycarbonyl)indoline-6-carboxylic acid serves as a versatile building block in medicinal chemistry, enabling efficient access to indoline-based scaffolds. The tert-butyl ester group provides excellent bench stability and facilitates straightforward deprotection under mild acidic conditions. It functions effectively in standard coupling reactions and supports the synthesis of complex heterocycles relevant to pharmaceutical 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 : H315-H319
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Precautionary Statements : P264-P280-P302+P352-P362
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Lot numbers can be found on the outside label of a product: