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Structure of 1818843-14-9
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tert-Butyl N-[(2R)-azetidin-2-ylmethyl]carbamate hydrochloride offers a stable, moisture-tolerant platform for introducing chiral azetidine units in synthetic sequences. The (2R)-configured azetidinylmethyl moiety integrates readily into bioactive scaffolds, while the tert-butyl carbamate group enables selective protection and orthogonal deprotection under mild conditions. This hydrochloride salt enhances solubility and handling in aqueous or polar organic media, streamlining downstream processing in medicinal chemistry workflows.
tert-Butyl N-[(2R)-azetidin-2-ylmethyl]carbamate hydrochloride serves as a stable, bench-ready building block for the synthesis of bioactive azetidine-containing scaffolds. The protected amine enables orthogonal functionalization in late-stage diversification, while the chiral (2R)-azetidin-2-ylmethyl moiety provides a well-defined stereochemical handle for medicinal chemistry campaigns. Its compatibility with standard coupling and reduction protocols facilitates efficient access to complex heterocyclic architectures.
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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: