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Structure of 63329-02-2
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(R)-4-tert-Butyl 1-methyl 2-aminosuccinate hydrochloride features a chiral succinate core with a tert-butyl and methyl substitution, delivering enhanced steric shielding and improved solubility in polar media. The protonated amine facilitates efficient salt formation, enabling robust handling and integration into asymmetric synthesis workflows. This bench-stable derivative supports direct use in peptide coupling and catalytic transformations.
(R)-4-tert-Butyl 1-methyl 2-aminosuccinate hydrochloride serves as a chiral building block for asymmetric synthesis, enabling stereoselective construction of biologically relevant scaffolds. The protected amine and ester functionalities offer orthogonal reactivity, facilitating sequential transformations in peptide-like and heterocyclic compound assembly. Bench-stable and readily purified, it functions effectively in standard synthetic workflows requiring controlled functionalization and high enantiomeric purity.
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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-P280-P302+P352
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Lot numbers can be found on the outside label of a product: