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Structure of 390766-89-9
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This imidazolidinone scaffold delivers a sterically encumbered, bench-stable chiral core ideal for asymmetric synthesis. The tert-butyl and benzyl substituents provide enhanced solubility and stability, while the rigid framework supports high diastereoselectivity in reductive amination and catalytic functionalization processes.
(2R,5R)-5-Benzyl-2-(tert-butyl)-3-methylimidazolidin-4-one serves as a robust chiral building block for the synthesis of bioactive heterocycles. Its tertiary amide functionality and sterically encumbered imidazolidinone core enable high diastereoselectivity in asymmetric transformations. The molecule exhibits excellent bench stability, facilitates straightforward purification, and demonstrates broad functional group tolerance in standard coupling and reduction protocols, making it a practical choice for medicinal chemistry campaigns and API intermediate development.
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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: