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Structure of 1956324-96-1
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tert-Butyl 4,6-dibromoindoline-1-carboxylate features a sterically hindered indoline core with bromine substituents at the 4- and 6-positions, enabling efficient late-stage functionalization in cross-coupling reactions. The tert-butyl ester group offers enhanced stability and ease of removal under mild acidic conditions, facilitating downstream derivatization. This compound serves as a key intermediate for the synthesis of biologically active indoline derivatives.
tert-Butyl 4,6-dibromoindoline-1-carboxylate serves as a versatile building block for the synthesis of brominated indoline scaffolds. Its dibromo substitution pattern enables sequential cross-coupling reactions, while the tert-butyl carbamate group offers stable protection under standard reaction conditions. The molecule exhibits excellent bench stability and facilitates straightforward deprotection, making it ideal for constructing complex heterocyclic architectures in medicinal chemistry and process development workflows.
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GHS Pictogram :
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GHS No : GHS06,GHS09
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Signal Word : Danger
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UN#: 2811
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Class : 6.1
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Packing Group : Ⅲ
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Hazard Statements : H301-H315-H319-H335-H410
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Precautionary Statements : P261-P264-P270-P271-P273-P280-P302+P352-P304+P340-P330-P362+P364-P391-P405-P501
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Lot numbers can be found on the outside label of a product: