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Structure of 195964-54-6
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This chiral pyrrolidine derivative features a tert-butyl-protected nitrogen and a methyl ester, enabling selective functionalization. The methoxy group enhances solubility and stabilizes the cyclic scaffold under standard conditions. Ideal for asymmetric synthesis and peptide backbone modification.
(2S)-1-tert-Butyl 2-methyl 5-methoxypyrrolidine-1,2-dicarboxylate serves as a stereocontrolled building block for pyrrolidine-based scaffolds in medicinal chemistry. Its tert-butyl and methyl ester groups enable selective deprotection and derivatization, while the methoxy substituent provides orthogonal functionalization potential. The compound exhibits bench stability and facilitates efficient synthesis of complex heterocycles through standard coupling and reduction protocols.
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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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: