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Structure of 879887-32-8
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tert-Butyl 5-formylindoline-1-carboxylate features a sterically shielded tert-butyl ester and a reactive aldehyde group at the indoline C5 position, enabling selective functionalization. The electron-rich indoline core supports transition metal-catalyzed transformations, while the formyl moiety facilitates conjugation reactions under mild conditions. This bench-stable scaffold integrates readily into complex molecular architectures.
tert-Butyl 5-formylindoline-1-carboxylate serves as a versatile building block for the synthesis of indoline-based pharmaceutical scaffolds. The formyl group enables direct functionalization via nucleophilic additions, while the protected amine facilitates subsequent coupling reactions. Its bench-stable nature and compatibility with standard transformations support efficient access to complex heterocycles in medicinal chemistry 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
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Precautionary Statements : P261-P280-P304+P340-P501
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Lot numbers can be found on the outside label of a product: