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Structure of 947141-86-8
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tert-Butyl trans-4-ethynylcyclohexylcarbamate features a rigid trans-cyclohexyl scaffold with a pendant ethynyl group, enabling efficient copper-catalyzed click reactions. The tert-butyl carbamate moiety provides stable protection for amine functionalities under standard conditions, while the electron-deficient alkyne facilitates selective coupling. This combination delivers robust, orthogonal functionalization in complex molecular architectures.
tert-Butyl trans-4-ethynylcyclohexylcarbamate serves as a versatile building block in synthetic organic chemistry, enabling efficient access to functionalized cyclohexyl scaffolds via copper-catalyzed azide-alkyne cycloaddition (CuAAC). The protected amine and terminal alkyne functionalities offer orthogonal reactivity for late-stage diversification. Its trans-configuration ensures defined stereochemistry, while the tert-butyl carbamate group provides excellent bench stability and ease of removal under mild acidic conditions.
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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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: