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Structure of 204711-97-7
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(S)-2-((tert-Butoxycarbonyl)amino)hept-6-enoic acid is a chiral building block featuring a terminal alkene and a protected amine, enabling selective conjugate additions and late-stage functionalization. The tert-butyl carbamate group ensures stability during synthetic manipulations, while the (S)-configuration provides stereocontrol in peptide-like architectures. This versatile intermediate supports efficient access to bioactive scaffolds under standard conditions.
(S)-2-((tert-Butoxycarbonyl)amino)hept-6-enoic acid serves as a versatile chiral building block for peptide synthesis and heterocyclic scaffold construction. The conjugated enoic acid moiety enables efficient Michael additions and Diels–Alder reactions, while the Boc-protected amine offers orthogonal functionality for sequential derivatization. Bench-stable and readily purified by flash chromatography, it facilitates scalable access to bioactive analogs in medicinal chemistry campaigns.
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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-H312-H332
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362+P364-P501
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Lot numbers can be found on the outside label of a product: