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Structure of 145106-43-0
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tert-Butyl N-[(1S,2S)-2-hydroxycyclopentyl]carbamate features a chiral cyclopentane scaffold with a hydroxyl group in the cis configuration, enabling stereocontrolled synthesis. The tert-butyloxycarbonyl (Boc) group provides robust protection for amine functionalities under acidic conditions. This bifunctional reagent integrates seamlessly into complex molecule assembly workflows, offering high stability and predictable reactivity in peptide and natural product synthesis.
tert-Butyl N-[(1S,2S)-2-hydroxycyclopentyl]carbamate serves as a versatile chiral building block for asymmetric synthesis, enabling efficient construction of cyclopentane-based scaffolds. The protected amine and secondary alcohol functionalities exhibit excellent bench stability and compatibility with standard coupling and functionalization protocols. Its orthogonal reactivity facilitates sequential transformations in complex molecule assembly, particularly in medicinal chemistry and natural product synthesis.
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GHS No : GHS07,GHS08,GHS09
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Signal Word : Danger
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UN#: 3077
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Class : 9
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Packing Group : Ⅲ
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Hazard Statements : H302-H372-H400
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Precautionary Statements : P260-P264-P273-P501
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Lot numbers can be found on the outside label of a product: