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Structure of 1083181-22-9
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This cyclopropanecarboxylic acid derivative features a carbamate-protected amine group, enabling stable incorporation into peptide synthesis workflows. The tert-butoxycarbonyl (Boc) moiety provides orthogonal protection, while the strained cyclopropane ring imparts unique conformational rigidity useful in bioactive molecule design.
2-[[(1,1-Dimethylethoxy)carbonyl]amino]cyclopropanecarboxylic acid serves as a stable, bench-ready building block for peptide synthesis and medicinal chemistry. The Boc-protected amino group enables selective deprotection under mild acidic conditions, while the cyclopropane ring imparts conformational rigidity useful in bioactive molecule design. Its compatibility with standard coupling protocols and ease of purification support efficient workflow integration in complex molecule assembly.
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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: