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Structure of 790667-49-1
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This tert-butyl ester derivative of (2S)-2-methyl-4-oxopiperidine-1-carboxylic acid features a chiral, bench-stable scaffold with a protected carboxylic acid. The piperidine core bears a ketone at C4 and a methyl group at C2, enabling direct incorporation into complex heterocycles. Its robust stability under standard conditions supports efficient use in synthetic sequences requiring selective transformations.
(2S)-2-Methyl-4-oxo-piperidine-1-carboxylic acid tert-butyl ester serves as a versatile chiral building block for the synthesis of bioactive heterocycles and pharmaceutical intermediates. Its tert-butyl carbamate group enables facile deprotection under mild acidic conditions, while the 4-oxo functionality supports nucleophilic addition and reductive amination reactions. The (2S)-configuration provides stereocontrol in asymmetric synthesis, and the compound exhibits excellent bench stability and compatibility with standard purification methods.
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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: