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CAS 390766-89-9

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(2R,5R)-5-benzyl-2-tert-butyl-3-methylimidazolidin-4-one

Description:
(2R,5R)-5-benzyl-2-tert-butyl-3-methylimidazolidin-4-one is a chiral imidazolidinone compound characterized by its unique structural features, including a five-membered ring containing nitrogen atoms. The presence of a tert-butyl group and a benzyl group contributes to its steric bulk and hydrophobic characteristics, which can influence its solubility and reactivity. This compound is typically used in organic synthesis and may serve as a chiral auxiliary or ligand in asymmetric catalysis due to its stereogenic centers. The imidazolidinone framework is known for its ability to stabilize certain reactive intermediates, making it valuable in various chemical transformations. Additionally, the specific stereochemistry (2R,5R) indicates the spatial arrangement of substituents, which is crucial for its biological activity and interaction with other molecules. Overall, this compound exemplifies the complexity and utility of chiral imidazolidinones in synthetic organic chemistry.
Formula:C15H22N2O
InChI:InChI=1/C15H22N2O/c1-15(2,3)14-16-12(13(18)17(14)4)10-11-8-6-5-7-9-11/h5-9,12,14,16H,10H2,1-4H3/t12-,14-/m1/s1
SMILES:CC(C)(C)[C@@H]1N[C@H](Cc2ccccc2)C(=O)N1C
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