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Comprehensive Overview of 1-Phenylimidazolidin-2-one (CAS No. 1848-69-7): Properties, Applications, and Industry Insights

1-Phenylimidazolidin-2-one (CAS No. 1848-69-7), a specialized organic compound, has garnered significant attention in pharmaceutical and chemical research due to its unique structural properties. This heterocyclic molecule features a phenyl group attached to an imidazolidin-2-one core, making it a versatile intermediate for synthesizing bioactive molecules. Researchers often search for "1-Phenylimidazolidin-2-one synthesis" or "CAS 1848-69-7 applications," reflecting its growing relevance in drug discovery and material science.

The compound's molecular formula (C9H10N2O) and weight (162.19 g/mol) align with its role as a building block for N-containing heterocycles. Its crystalline form and moderate solubility in polar solvents like ethanol or DMSO make it suitable for controlled reactions. Recent studies highlight its potential in designing kinase inhibitors and neurological agents, addressing trending topics such as "small molecule therapeutics" and "targeted drug delivery."

From an industrial perspective, 1-Phenylimidazolidin-2-one is pivotal in optimizing "green chemistry" processes. Manufacturers increasingly seek "sustainable synthesis routes for CAS 1848-69-7" to reduce environmental impact, aligning with global ESG (Environmental, Social, and Governance) trends. Advanced catalytic methods, including microwave-assisted reactions, have improved its production efficiency while minimizing waste.

Analytical characterization of this compound typically involves HPLC, NMR spectroscopy, and mass spectrometry, ensuring high purity (>98%) for research applications. Its stability under ambient conditions makes it a reliable candidate for long-term storage, though inert atmospheres are recommended for extended periods. Users frequently inquire about "1-Phenylimidazolidin-2-one safety data" and "handling precautions," emphasizing the need for transparent technical documentation.

In material science, derivatives of 1848-69-7 exhibit promising optical properties, spurring interest in "organic electronic materials" and "photoactive polymers." The compound's ability to modify electron density in conjugated systems supports innovations in OLEDs and sensors. Patent analyses reveal a steady rise in filings incorporating this scaffold, particularly in Asia-Pacific markets.

Regulatory compliance remains a key focus, with REACH and FDA guidelines governing its use in end products. Suppliers emphasizing "GMP-grade 1-Phenylimidazolidin-2-one" cater to pharmaceutical clients requiring stringent quality controls. The compound's non-hazardous classification under standard handling conditions enhances its adoption across labs.

Future research directions may explore 1-Phenylimidazolidin-2-one's role in covalent organic frameworks (COFs) or bioconjugation techniques. With AI-driven molecular modeling accelerating discovery, queries like "CAS 1848-69-7 in silico studies" are becoming prevalent. Collaborative efforts between academia and industry continue to unlock novel applications for this multifaceted compound.

• 102063-87-6(Urea, N'-(2-aminoethyl)-N-methyl-N-phenyl-)
• 4474-03-7(Urea,N-ethyl-N'-methyl-N,N'-diphenyl-)
• 54924-46-8(ethylene diurea)
• 89518-99-0(1-(4-aminophenyl)imidazolidin-2-one)
• 85-98-3(1,3-Diethyl-1,3-diphenylurea)
• 65173-07-1(1-[2-(n-methylanilino)ethyl]-3-phenylurea)
• 89518-36-5(Acetamide, N-[4-(2-oxo-1-imidazolidinyl)phenyl]-)
• 64544-71-4(Urea,N-ethyl-N,N'-diphenyl-)
• 517918-82-0(1-(3-Aminophenyl)-3-methylimidazolidin-2-one)
• 62898-93-5(1,1'-carbonylbis(3-phenylimidazolidin-2-one))