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Structure of 936829-23-1
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tert-Butyl 3-aminoindoline-1-carboxylate features a sterically hindered tert-butyl ester that enhances stability and facilitates straightforward deprotection. The aminoindoline core provides a versatile scaffold for medicinal chemistry, integrating readily into complex heterocycles. This bench-stable compound enables efficient access to bioactive indoline derivatives under standard conditions.
tert-Butyl 3-aminoindoline-1-carboxylate serves as a versatile building block for the synthesis of indoline-based pharmaceutical scaffolds. Its tert-butyl carbamate group provides excellent stability and ease of removal under mild acidic conditions, while the primary amine enables direct functionalization or coupling reactions. The molecule exhibits robust compatibility with standard synthetic transformations, facilitating access to complex heterocycles relevant in medicinal chemistry and process 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 : 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: