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Structure of 1352709-57-9
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(S)-2-(Morpholin-2-yl)acetic acid hydrochloride features a chiral morpholine-bearing side chain, offering enhanced solubility and metabolic stability. This bench-stable derivative integrates readily into peptide-based conjugates and bioactive molecule scaffolds. The hydrochloride salt form improves handling and crystallization behavior in synthetic workflows.
(S)-2-(Morpholin-2-yl)acetic acid hydrochloride serves as a versatile chiral building block in medicinal chemistry, enabling the synthesis of bioactive molecules through established amide and ester coupling reactions. Its morpholine moiety provides enhanced solubility and hydrogen-bonding capacity, while the α-chiral center supports stereoselective transformations. The hydrochloride salt ensures excellent bench stability and ease of handling, facilitating purification and integration into multi-step synthetic sequences.
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Lot numbers can be found on the outside label of a product: