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Structure of 180307-56-6
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tert-Butyl 4-vinylpiperidine-1-carboxylate, stabilized with MEHQ, features a reactive vinyl group enabling efficient incorporation into polymer architectures and conjugation workflows. The tert-butyl ester moiety provides stability and ease of deprotection under mild acidic conditions. This bench-stable, moisture-tolerant reagent facilitates rapid access to functionalized piperidines in synthetic and medicinal chemistry applications.
tert-Butyl 4-vinylpiperidine-1-carboxylate serves as a versatile building block in synthetic organic chemistry, enabling efficient access to functionalized piperidine scaffolds via palladium-catalyzed cross-coupling reactions. The vinyl group facilitates reliable Heck, Suzuki-Miyaura, and Sonogashira transformations, while the tert-butyl carbamate (Boc) group provides orthogonal protection for nitrogen. This reagent exhibits excellent bench stability and ease of purification, making it well-suited for medicinal chemistry campaigns and API intermediate 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: