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Structure of 2102410-18-2
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This bench-stable, moisture-tolerant carbamate derivative features a stereodefined pyrrolidine core with a tert-butyl-protected amine. It serves as a key chiral building block in asymmetric synthesis, enabling efficient access to complex nitrogen-containing scaffolds through selective deprotection and coupling reactions.
rel-tert-Butyl ((3R,4R)-4-methylpyrrolidin-3-yl)carbamate hydrochloride serves as a stable, bench-ready chiral building block for the synthesis of pyrrolidine-based scaffolds. Its well-defined stereochemistry enables predictable outcomes in asymmetric synthesis, while the tert-butyl carbamate group provides excellent protection and ease of removal under mild acidic conditions. The molecule exhibits robust functional group tolerance and facilitates efficient incorporation into diverse medicinal chemistry workflows, including peptide extensions and heterocyclic ring formations.
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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: