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MSE PRO 1-Phenylimidazolidin-2-one, ≥97.0% Purity– MSE Supplies LLC

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MSE PRO 1-Phenylimidazolidin-2-one, ≥97.0% Purity - MSE Supplies LLC

MSE PRO 1-Phenylimidazolidin-2-one, ≥97.0% Purity

SKU: CM1391

  • $ 30995

MSE PRO™ 1-Phenylimidazolidin-2-one, ≥97.0% Purity

MSE PRO™ 1-Phenylimidazolidin-2-one is a captivating heterocyclic compound that combines the structural elements of an imidazolidine ring and a phenyl substituent, creating a molecular scaffold with remarkable synthetic potential. This compound boasts a distinctive molecular architecture, featuring a five-membered imidazolidine ring fused with an aromatic phenyl group. This structural motif introduces intriguing chemical properties and reactivity profiles, making it an attractive building block for organic synthesis and medicinal chemistry endeavors.

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

Technical Specifications:

CAS No. 1848-69-7
Chemical name 1-Phenylimidazolidin-2-one
Synonym(s)
  • 1-phenyl-imidazolidin-2-one
  • 1-Phenyl-2-imidazolidinone
Molecular formula C9H10N2O      
Pack size 1 g (CM1391)
Molecular weight 162.19 g/mol
Purity ≥97.0% (NMR) 
Melting point 68 °C
Density   1.188±0.06 g/cm3 (Predicted)
pKa 14±0.20 (Predicted)
Appearance White to off-white solid
Storage  Store at temperature 2-8 °C


References:

[1] Krylov, C. S., Komogortsev, A. N., Lichitsky, B. V., Fakhrutdinov, A. N., Dudinov, A. А., & Krayushkin, M. M. (2019). Three-Component Condensation of 4-Imino-1-Phenylimidazolidin-2-One with Aldehydes and Meldrum's Acid: Synthesis of Imidazo [4, 5-b] Pyridine-2, 5 (4 H, 6 H)-Diones and 5-Substituted 1-Phenylhydantoins. Chemistry of Heterocyclic Compounds, 55, 851-855.

[2] A Ammar, Y., AM Sh El-Sharief, M., M Ghorab, M., A Mohamed, Y., Ragab, A., & Y Abbas, S. (2016). New imidazolidineiminothione, imidazolidin-2-one and imidazoquinoxaline derivatives: Synthesis and evaluation of antibacterial and antifungal activities. Current Organic Synthesis, 13(3), 466-475.