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MSE PRO (S)-5-Benzyl-2,2,3-trimethylimidazolidin-4-one, ≥95.0% Purity– MSE Supplies LLC

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MSE PRO (S)-5-Benzyl-2,2,3-trimethylimidazolidin-4-one, ≥95.0% Purity - MSE Supplies LLC

MSE PRO (S)-5-Benzyl-2,2,3-trimethylimidazolidin-4-one, ≥95.0% Purity

SKU: CM1386

  • $ 75995
  • Save $ 9105

MSE PRO™ (S)-5-Benzyl-2,2,3-trimethylimidazolidin-4-one, ≥95.0% Purity

MSE PRO™ (S)-5-Benzyl-2,2,3-trimethylimidazolidin-4-one is a highly valuable and versatile chemical building block with significant potential in the pharmaceutical and fine chemicals industries. The unique structural features of this molecule make it an attractive target for a wide range of synthetic applications. The compound has a defined stereochemistry, with a single stereocenter in the (S)-configuration. This stereochemical purity is crucial for many pharmaceutical and asymmetric synthesis applications, where the specific spatial arrangement of atoms can have a dramatic impact on the desired biological activity or reaction outcomes.

MSE Supplies offers various N-heterocyclic drug small molecules and other chemical reagents. Please contact us for bulk orders.

Technical Specifications:

CAS No. 132278-63-8
Chemical name (S)-5-Benzyl-2,2,3-trimethylimidazolidin-4-one
Synonym(s)
  • (5S)-2,2,3-TriMethyl-5-benzyl-4-imidazolidinone
  • (5S)-2,2,3-Trimethyl-5-(phenylmethyl)-4-imidazolidinone
Molecular formula C13H18N2O    
Pack size

5 g (CM1386)
Molecular weight 218.29 g/mol
Purity ≥95.0% (NMR) 
Boiling point 351.0±35.0 °C (Predicted)
Density   1.044±0.06 g/cm3 (Predicted)
pKa 5.65±0.60 (Predicted)
Appearance Colorless to light yellow (Viscous liquid)
Storage  2-8 °C, protect from light


References:

[1] Park, J. K., Sreekanth, P., & Kim, B. M. (2004). Recycling chiral Imidazolidin‐4‐one catalyst for asymmetric Diels–Alder reactions: screening of various ionic liquids. Advanced Synthesis & Catalysis, 346(1), 49-52.

[2] Burley, J. C., Gilmour, R., Prior, T. J., & Day, G. M. (2008). Structural diversity in imidazolidinone organocatalysts: a synchrotron and computational study. Acta Crystallographica Section C: Crystal Structure Communications, 64(1), o10-o14.