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Structure of 362706-26-1
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This sterically hindered pyrrolidine derivative features a tert-butyl group and methyl substituent that enhance solubility and stability. The 4-oxo functionality enables direct participation in cycloadditions and conjugate additions, while the dicarboxylate moiety supports orthogonal functionalization. Designed for synthetic efficiency in complex molecule assembly.
1-(tert-Butyl) 2-methyl 4-oxopyrrolidine-1,2-dicarboxylate serves as a versatile pyrrolidine scaffold builder in synthetic organic chemistry. Its stability under standard reaction conditions enables efficient functionalization at the C4 carbonyl and C2 methyl positions. The tert-butyl ester group facilitates straightforward deprotection, while the dicarboxylate framework supports diverse transformations including reductive amination and cycloaddition reactions. This compound functions as a key intermediate in the construction of bioactive heterocycles and peptidomimetics.
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GHS No : GHS05
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Signal Word : Danger
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UN#: 1760
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Class : 8
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Packing Group : Ⅲ
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Hazard Statements : H302-H315-H318-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362-P405-P501
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Lot numbers can be found on the outside label of a product: