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Structure of 1638765-05-5
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tert-Butyl N-[3-(aminomethyl)bicyclo[1.1.1]pentan-1-yl]carbamate features a rigid, strain-engineered bicyclo[1.1.1]pentane scaffold that imparts exceptional metabolic stability and conformational restriction. The pendant aminomethyl group enables direct functionalization or coupling in late-stage diversification. This carbamate-protected amine is bench-stable and compatible with standard peptide synthesis protocols.
tert-Butyl N-[3-(aminomethyl)bicyclo[1.1.1]pentan-1-yl]carbamate serves as a stable, bench-friendly amino carbamate building block for medicinal chemistry and synthetic applications. The bicyclo[1.1.1]pentane core imparts exceptional rigidity and metabolic stability, while the tert-butyl carbamate group enables selective protection of primary amines. It facilitates efficient incorporation into complex scaffolds via standard coupling reactions and tolerates diverse functional groups, simplifying purification and enabling direct use in peptide and small-molecule synthesis workflows.
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GHS Pictogram :
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GHS No : GHS05,GHS07
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Signal Word : Danger
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UN#: 3259
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Class : 8
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Packing Group : Ⅲ
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Hazard Statements : H315-H318-H335
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Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: