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Structure of 132278-63-8
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This chiral imidazolidinone features a sterically hindered core with a benzyl group at the 5-position, enabling selective reactivity in asymmetric synthesis. The trimethyl substitution enhances stability and solubility, while the lactam scaffold provides a rigid framework for stereocontrol. Ideal for constructing complex nitrogen-containing architectures under mild conditions.
(S)-5-Benzyl-2,2,3-trimethylimidazolidin-4-one serves as a chiral building block for the synthesis of bioactive heterocycles and pharmaceutical intermediates. Its rigid imidazolidinone core offers excellent functional group tolerance and bench stability, enabling efficient transformations in standard coupling and reduction protocols. The stereogenic center supports enantioselective synthesis, while the benzyl and methyl substituents enhance solubility and reactivity in diverse reaction environments.
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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: