1214998-34-1

Basic information

• Product Name: 3-cyclohexyl-5-(4-methoxyphenyl)oxazolidin-2-one
• Synonyms: 3-cyclohexyl-5-(4-methoxyphenyl)oxazolidin-2-one
• CAS NO: 1214998-34-1
• Molecular Weight: 275.348
• Mol File: 1214998-34-1.mol

Chemical Properties

• CAS DataBase Reference: 3-cyclohexyl-5-(4-methoxyphenyl)oxazolidin-2-one(CAS DataBase Reference)
• NIST Chemistry Reference: 3-cyclohexyl-5-(4-methoxyphenyl)oxazolidin-2-one(1214998-34-1)
• EPA Substance Registry System: 3-cyclohexyl-5-(4-methoxyphenyl)oxazolidin-2-one(1214998-34-1)

Safety Data

• Hazardous Substances Data: 1214998-34-1(Hazardous Substances Data)

Upstream product

• 124-38-9 carbon dioxide 
• 1214998-31-8 C₁₅H₂₁NO 

Relevant articles and documents

Naturally occurring α-amino acid: a simple and inexpensive catalyst for the selective synthesis of 5-aryl-2-oxazolidinones from CO2 and aziridines under solvent-free conditions

Naturally occurring α-amino acid successfully catalyzed cycloaddition of aziridine with carbon dioxide to afford 5-aryl-2-oxazolisinones under mild conditions without the need of any additives. The scope of this reaction is very general, providing the corresponding products in good yields and excellent regioselectivity (87:13-100:0) regardless of the α-amino acid examined and a wide variety of N-substituted aziridines employed. Two possible reaction pathways for the reaction were also discussed.

Polystyrene-supported amino acids as efficient catalyst for chemical fixation of carbon dioxide

Four new polystyrene-supported amino acids have been synthesized and applied to the chemical fixation of carbon dioxide for the first time. Two series of experiments with polystyrene-supported threonine (PS-Thr) and polystyrene-supported tyrosine (PS-Tyr) as catalyst, respectively, were conducted to study the effect of the reaction conditions on the carboxylation of propylene oxide/carbon dioxide. There was no considerable decrease in the yield of propylene carbonate after the polystyrene-supported amino acids were used five times, indicating that these catalysts are very stable. It was demonstrated that these catalysts were very efficient in the carboxylation of various epoxides and aziridines with carbon dioxide under mild conditions without any solvents. The mechanism for this carboxylation is also discussed.