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Structure of 136092-76-7
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(S)-2-((tert-Butoxycarbonyl)(methyl)amino)pent-4-enoic acid features a stabilized enoic acid backbone with a tert-butoxycarbonyl-protected amine and methyl substitution, enabling direct incorporation into peptide synthesis workflows. The conjugated double bond facilitates efficient coupling reactions under standard conditions. This bench-stable derivative, preserved with MEHQ, maintains reactivity while minimizing decomposition during storage and handling.
(S)-2-((tert-Butoxycarbonyl)(methyl)amino)pent-4-enoic acid serves as a versatile chiral building block for peptide and heterocyclic synthesis. The conjugated enoic acid functionality enables efficient Michael additions and palladium-catalyzed couplings, while the Boc-methylamino group offers orthogonal protection. Stabilized with MEHQ, it exhibits enhanced bench stability and facilitates straightforward purification, making it well-suited for iterative synthetic sequences in medicinal chemistry and process development.
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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-P363-P501
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Lot numbers can be found on the outside label of a product: