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Structure of 645400-44-8
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tert-Butyl ((1S,3S)-3-aminocyclopentyl)carbamate delivers a chiral cyclopentyl scaffold with a protected amine for stereoselective synthesis. This bench-stable carbamate anchors diverse functionalizations in medicinal chemistry and peptide analog development. The (1S,3S) configuration ensures high diastereoselectivity in downstream transformations.
tert-Butyl ((1S,3S)-3-aminocyclopentyl)carbamate serves as a versatile chiral building block for the synthesis of bioactive molecules. The (1S,3S)-configured cyclopentylamine moiety enables stereoselective transformations, while the tert-butyl carbamate group provides excellent bench stability and facilitates straightforward deprotection under mild acidic conditions. Its functional group tolerance supports diverse coupling reactions, making it well-suited for medicinal chemistry applications and API 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: