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Structure of 369595-01-7
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tert-Butyl 3-oxoindoline-1-carboxylate features a sterically hindered tert-butyl ester group that enhances stability and simplifies purification. The molecule integrates a fused indoline scaffold with a ketone at the 3-position, enabling direct functionalization in synthetic sequences. This combination supports efficient access to complex heterocyclic architectures under standard conditions.
tert-Butyl 3-oxoindoline-1-carboxylate serves as a versatile building block in synthetic organic chemistry, enabling efficient access to indoline-based scaffolds prevalent in medicinal chemistry. The molecule combines a readily reducible ketone with a stable carbamate-protected amine, offering orthogonal functional group reactivity. It facilitates reductive amination, nucleophilic addition, and transition-metal-catalyzed coupling reactions under mild conditions. Its bench-stable nature and ease of purification support scalable synthesis of complex heterocycles and API intermediates.
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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: