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Structure of 34582-30-4
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(S)-1-tert-Butyl 4-methyl 2-aminosuccinate hydrochloride features a chiral succinate core with a tert-butyl ester and methyl substituent, delivering a bench-stable, moisture-tolerant scaffold for asymmetric synthesis. The protonated amine enhances solubility in polar solvents, enabling efficient coupling reactions in peptide analog development and catalyst design.
(S)-1-tert-Butyl 4-methyl 2-aminosuccinate hydrochloride serves as a chiral building block for the synthesis of bioactive molecules, enabling efficient access to pyrrolidine and piperidine derivatives via reductive amination or cyclization. The protected amine and ester functionalities offer excellent functional group tolerance, facilitating downstream transformations in medicinal chemistry campaigns. Its bench-stable solid form simplifies handling and purification in multi-step syntheses.
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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: