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Structure of 114214-71-0
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tert-Butyl 3-methylidenepyrrolidine-1-carboxylate features a stabilized enol ether moiety flanked by a pyrrolidine ring, enabling direct incorporation into cascade cyclizations and transition-metal-catalyzed transformations. This bench-stable, moisture-tolerant building block facilitates rapid access to nitrogen-containing heterocycles under standard conditions.
tert-Butyl 3-methylidenepyrrolidine-1-carboxylate serves as a versatile pyrrolidine-based building block in synthetic organic chemistry, enabling efficient access to substituted pyrrolidines via mild acid-mediated deprotection or Michael addition. The exocyclic methylene group facilitates conjugate addition reactions, while the tert-butoxycarbonyl (Boc) group provides robust protection under standard conditions. Its bench-stable nature and compatibility with diverse functional groups make it well-suited for medicinal chemistry campaigns and multistep synthesis.
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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: