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Structure of 219803-57-3
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(S)-2-Aminobut-3-en-1-ol hydrochloride, stabilized with MEHQ, features a chiral allylic amine scaffold with enhanced shelf stability. This bench-stable derivative supports stereoselective synthesis in medicinal chemistry workflows, offering reliable reactivity for the construction of complex nitrogen-containing architectures under standard conditions.
(S)-2-Aminobut-3-en-1-ol hydrochloride serves as a chiral building block for synthesizing bioactive molecules, enabling efficient access to β-amino alcohol scaffolds via reductive amination or conjugate addition. The stabilized form (with MEHQ) enhances bench stability and facilitates handling during multistep syntheses. Its functional group tolerance supports downstream transformations including amide formation and cyclization reactions, making it valuable in medicinal chemistry and peptide-like compound 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-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: