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Structure of 146394-99-2
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tert-Butyl (E)-(4-aminobut-2-en-1-yl)carbamate features a stable, bench-stable enamine moiety flanked by a protected amine and a conjugated double bond. This versatile scaffold integrates readily into synthetic sequences requiring selective functionalization, particularly in the construction of bioactive intermediates and peptidomimetics. The (E)-configuration ensures predictable stereochemical outcomes in downstream transformations.
tert-Butyl (E)-(4-aminobut-2-en-1-yl)carbamate serves as a versatile synthetic intermediate for the construction of bioactive heterocycles and peptide-like scaffolds. The conjugated enamine functionality enables efficient Michael additions and transition-metal-catalyzed couplings, while the tert-butoxycarbonyl (Boc) group provides stable protection of the primary amine under standard reaction conditions. Its bench-stable nature and compatibility with diverse functional groups facilitate straightforward purification and integration into multi-step syntheses.
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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: