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Structure of 454709-98-9
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tert-Butyl N-[cis-3-aminocyclopentyl]carbamate delivers a protected amine handle on a rigid cis-cyclopentyl scaffold, enabling direct incorporation into cyclic peptide architectures. The tert-butyl carbamate group ensures stable protection under standard conditions while facilitating straightforward deprotection via mild acidolysis. This compound features high configurational stability and is particularly suited for the synthesis of constrained bioactive peptides.
tert-Butyl N-[cis-3-aminocyclopentyl]carbamate serves as a versatile building block in medicinal chemistry, enabling direct incorporation of a cis-3-aminocyclopentyl moiety into target molecules. The carbamate group provides robust protection for the primary amine, offering excellent bench stability and compatibility with standard coupling reactions. Its functional group tolerance facilitates efficient late-stage diversification, while the rigid cyclopentyl scaffold imparts defined stereochemistry—ideal for structure-activity studies and macrocyclic scaffold construction.
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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: