Atomfair CID 839348 C12H14N2O3

Description CID 839348 (CAS No. 65855-02-9) is a high-purity organic compound with the molecular formula C12H14N2O3, systematically named as (5R)-1-benzyl-5-ethoxyimidazolidine-2,4-dione . This chiral imidazolidinedione derivative is meticulously synthesized for research applications, offering exceptional chemical stability and consistent batch-to-batch reproducibility. Its structural features include a benzyl group at the N1 position and an ethoxy substituent at the C5 position, making it a valuable intermediate in pharmaceutical and biochemical studies. Provided as a crystalline solid (??95% purity by HPLC), it is ideal for asymmetric synthesis, enzyme inhibition assays, and medicinal chemistry projects. Packaged under inert gas in amber glass vials to ensure…

Description

Description

CID 839348 (CAS No. 65855-02-9) is a high-purity organic compound with the molecular formula C12H14N2O3, systematically named as (5R)-1-benzyl-5-ethoxyimidazolidine-2,4-dione. This chiral imidazolidinedione derivative is meticulously synthesized for research applications, offering exceptional chemical stability and consistent batch-to-batch reproducibility. Its structural features include a benzyl group at the N1 position and an ethoxy substituent at the C5 position, making it a valuable intermediate in pharmaceutical and biochemical studies. Provided as a crystalline solid (??95% purity by HPLC), it is ideal for asymmetric synthesis, enzyme inhibition assays, and medicinal chemistry projects. Packaged under inert gas in amber glass vials to ensure long-term stability. SDS and analytical certificates available upon request.

  • CAS No: 65855-02-9
  • Molecular Formula: C12H14N2O3
  • Molecular Weight: 234.25
  • Exact Mass: 234.10044231
  • Monoisotopic Mass: 234.10044231
  • IUPAC Name: (5R)-1-benzyl-5-ethoxyimidazolidine-2,4-dione
  • SMILES: CCO[C@@H]1C(=O)NC(=O)N1CC2=CC=CC=C2
  • Synonyms: EC 417-340-4, SCHEMBL7498416, D88980

Application

CID 839348 serves as a key chiral building block in the synthesis of pharmacologically active compounds, particularly in the development of enzyme inhibitors targeting hydantoinase pathways. Researchers utilize this compound in asymmetric catalysis studies due to its rigid imidazolidinedione core and stereocenter. It has shown preliminary activity in modulating GABAA receptor function in neurological research models. The ethoxy group enhances solubility for organic-aqueous mixed solvent systems in reaction optimization.

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