Description
2,4-Imidazolidinedione, 5-ethoxy-1-(phenylmethyl)- (CAS No. 65855-02-9) is a high-purity organic compound with the molecular formula C12H14N2O3. This specialized chemical is widely utilized in pharmaceutical research, organic synthesis, and biochemical applications due to its unique imidazolidinedione core structure and benzyl-ethoxy substitution pattern. The product is rigorously tested for quality, ensuring >98% purity by HPLC analysis, and is supplied as a white to off-white crystalline powder. It is stable under recommended storage conditions (2-8°C in a tightly sealed container) and is soluble in common organic solvents including DMSO, methanol, and ethanol. Ideal for medicinal chemistry applications, this compound serves as a key intermediate in the development of novel therapeutic agents and as a reference standard in analytical studies.
Properties
- CAS Number: 65855-02-9
- Complexity: 300
- IUPAC Name: 1-benzyl-5-ethoxy-imidazolidine-2,4-dione
- InChI: InChI=1S/C12H14N2O3/c1-2-17-11-10(15)13-12(16)14(11)8-9-6-4-3-5-7-9/h3-7,11H,2,8H2,1H3,(H,13,15,16)
- InChI Key: FUQZCDCFSMSNBP-UHFFFAOYSA-N
- Exact Mass: 234.10044231
- Molecular Formula: C12H14N2O3
- Molecular Weight: 234.25
- SMILES: CCOC1C(=O)NC(=O)N1CC2=CC=CC=C2
- Topological: 58.6
- Monoisotopic Mass: 234.10044231
- Solubility: 29.8 [ug/mL]
- Synonyms: 1-benzyl-5-ethoxyimidazolidine-2,4-dione, 2,4-Imidazolidinedione, 5-ethoxy-1-(phenylmethyl)-, DTXSID60886786, DTXCID101026105, 417-340-4, 65855-02-9, 1-Benzyl-5-ethoxyhydantoin, 1-Benzyl-5-ethoxy-imidazolidine-2,4-dione, (5R)-1-benzyl-5-ethoxyimidazolidine-2,4-dione, 1-benzyl-5-ethoxy-2,4-imidazolidinedione, 1-Benzyl-5-ethoxy-2,4-imidazolinedione, 1-benzyl-5-ethoxy-2,4-imidazolidine dione, MFCD03838588, MLS001180804, SCHEMBL3627524, SCHEMBL5886077, SCHEMBL9631715, SCHEMBL9631717, CHEMBL1550956, FUQZCDCFSMSNBP-UHFFFAOYSA-N, HMS2817E22, AKOS015888815, SB38169, NCGC00247235-01, AC-14405, AS-64543, SMR000477431, B3085, NS00077644, AN-974/42099356
This compound is primarily used as a synthetic intermediate in pharmaceutical research, particularly in the development of hydantoin derivatives with potential biological activity. Researchers employ it in structure-activity relationship studies for CNS-targeting compounds. The ethoxy and benzyl substitutions make it valuable for probing enzyme-substrate interactions in medicinal chemistry applications. It may also serve as a building block for more complex heterocyclic systems in drug discovery programs.
Safety and Hazards
GHS Hazard Statements
- H302: Harmful if swallowed [Warning Acute toxicity, oral]
Precautionary Statements
- P264, P270, P301+P317, P330, and P501
Hazard Classes and Categories
- Acute Tox. 4 (100%)
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