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Structure of 184719-80-0
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(R)-tert-Butyl pyrrolidine-2-carboxylate hydrochloride features a chiral pyrrolidine core with a bench-stable tert-butyl ester and protonated nitrogen, enabling direct use in asymmetric synthesis. This protected amino acid derivative integrates seamlessly into peptide coupling workflows, offering high diastereoselectivity and compatibility with standard reaction conditions.
(R)-tert-Butyl pyrrolidine-2-carboxylate hydrochloride serves as a stereochemically defined building block for the synthesis of bioactive heterocycles and peptidomimetics. Its stable, bench-ready form enables straightforward incorporation into iterative coupling reactions, with the protected amine exhibiting excellent functional group tolerance and compatibility with standard deprotection protocols. The chiral pyrrolidine core facilitates access to conformationally restricted scaffolds relevant in medicinal chemistry.
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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: