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Structure of 2096992-27-5
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This bicyclic scaffold features a protected amino group and a pendant acetic acid, enabling direct conjugation or further functionalization. The tert-butyl carbamate moiety provides stability during synthesis, while the rigid cage structure imparts conformational restraint ideal for peptide mimetics and bioactive molecule design under standard conditions.
This compound serves as a versatile building block for peptide and peptidomimetic synthesis, leveraging the rigid bicyclo[1.1.1]pentane scaffold to enhance metabolic stability and conformational control. The tert-butoxycarbonyl (Boc) group provides reliable protection of the amine, enabling orthogonal deprotection in standard synthetic workflows. The pendant acetic acid functionality facilitates conjugation via amide bond formation, while the overall structure exhibits excellent bench stability and compatibility with diverse reaction conditions.
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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: