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Structure of 214610-10-3
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tert-Butyl 2-oxoindoline-1-carboxylate features a bench-stable carbamate protecting group that enables reliable access to functionalized indoline scaffolds. The electron-deficient oxo group facilitates nucleophilic addition and cyclization reactions under mild conditions, while the tert-butyl moiety ensures compatibility with standard deprotection protocols. This compound serves as a key intermediate in the synthesis of biologically active indoline derivatives.
tert-Butyl 2-oxoindoline-1-carboxylate serves as a versatile building block in synthetic organic chemistry, enabling efficient access to indoline scaffolds via reductive amination or catalytic hydrogenation. The tert-butyl carbamate group provides excellent stability and facilitates straightforward deprotection under mild acidic conditions. Its compatibility with diverse functional groups and utility in constructing biologically relevant heterocycles make it a practical choice for medicinal chemistry and process 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-H317
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Precautionary Statements : P261-P264-P270-P272-P280-P302+P352-P330-P362+P364-P501
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Lot numbers can be found on the outside label of a product: