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Structure of 1914155-12-6
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tert-Butyl (4-aminobut-2-en-1-yl)carbamate hydrochloride delivers a protected aminoalkene handle for late-stage functionalization. The electron-rich enamine moiety enables efficient coupling reactions, while the tert-butyl carbamate group offers robust protection under standard conditions. This bench-stable derivative facilitates modular synthesis of complex nitrogen-containing scaffolds in medicinal chemistry and peptide conjugation workflows.
tert-Butyl (4-aminobut-2-en-1-yl)carbamate hydrochloride serves as a versatile building block in synthetic organic chemistry, enabling efficient access to functionalized amine intermediates. The protected amine and terminal alkene functionalities offer orthogonal reactivity for subsequent transformations, including cross-coupling, hydrogenation, and Michael additions. Its stability under standard bench conditions and ease of purification make it well-suited for iterative synthesis workflows in medicinal chemistry and process development.
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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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: