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Structure of 229613-83-6
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This methyl (1S,4R)-4-aminocyclopent-2-ene-1-carboxylate hydrochloride delivers a chiral, electron-rich cyclopentenyl scaffold with a bench-stable ammonium functionality. The para-amine moiety enables direct incorporation into peptidomimetic architectures and asymmetric synthesis workflows. Designed for efficient coupling under mild conditions, it serves as a high-purity building block in medicinal chemistry and catalytic reaction development.
Methyl (1S,4R)-4-aminocyclopent-2-ene-1-carboxylate hydrochloride serves as a stereochemically defined building block for nitrogen-containing heterocycles and bioactive molecule synthesis. The protected amine and enolizable carbonyl enable diverse transformations, including reductive amination, cyclization, and transition-metal-catalyzed coupling. Bench-stable and readily purified, it functions effectively in peptide-like scaffold construction and medicinal chemistry campaigns requiring controlled stereochemistry and functional group compatibility.
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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-P280-P302+P352
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Lot numbers can be found on the outside label of a product: