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Structure of 774212-81-6
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tert-Butyl ((1R,3S)-3-aminocyclopentyl)carbamate delivers a chiral cyclopentane scaffold with a selectively protected amine, enabling direct incorporation into asymmetric synthesis. The tert-butyl carbamate group ensures stability and ease of removal under mild acidic conditions, while the (1R,3S) stereochemistry provides defined spatial orientation for downstream functionalization in medicinal chemistry and peptide mimetics.
tert-Butyl ((1R,3S)-3-aminocyclopentyl)carbamate serves as a versatile chiral building block for the synthesis of bioactive cyclopentane-containing compounds. The protected amine enables selective functionalization at the 3-position of the cyclopentane ring, with the tert-butyl carbamate group offering excellent stability and ease of removal under mild acidic conditions. Its defined stereochemistry supports efficient asymmetric synthesis, while broad functional group tolerance facilitates integration into diverse coupling and cyclization workflows common 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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: