121485-50-5

Basic information

• Product Name: 3-(4-Methoxyphenyl)-5-methyl-2-oxazolidinone
• Synonyms: 3-(4-Methoxyphenyl)-5-methyl-2-oxazolidinone
• CAS NO: 121485-50-5
• Molecular Weight: 207.229
• Mol File: 121485-50-5.mol
• Article Data: 16

Chemical Properties

• CAS DataBase Reference: 3-(4-Methoxyphenyl)-5-methyl-2-oxazolidinone(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(4-Methoxyphenyl)-5-methyl-2-oxazolidinone(121485-50-5)
• EPA Substance Registry System: 3-(4-Methoxyphenyl)-5-methyl-2-oxazolidinone(121485-50-5)

Safety Data

• Hazardous Substances Data: 121485-50-5(Hazardous Substances Data)

Upstream product

• 5416-93-3 4-Methoxyphenyl isocyanate 
• 75-56-9 methyloxirane 
• 108-32-7 1,2-propylene cyclic carbonate 
• 62-53-3 aniline 
• 894693-94-8 1-((4-methoxyphenyl)amino)propan-2-ol 
• 124-38-9 carbon dioxide 
• 26198-63-0 1,2-Dichloropropane 
• 104-94-9 4-methoxy-aniline 
• 14803-72-6 methyl N-(4-methoxyphenyl)carbamate 
• 1359874-37-5 benzyl allyl(4-methoxyphenyl)carbamate 
• 7451-55-0 ethyl 4-methoxyphenylcarbamate 
• 102-09-0 bis(phenyl) carbonate 
• 42902-32-9 5-(hydroxy-methyl)-3-p-methoxyphenyl-2-oxazolidinone 
• 121082-86-8 5-(Bromomethyl)-3-(4-methoxyphenyl)-2-oxazolidinone 

Relevant articles and documents

Catalytic Dealkylative Synthesis of Cyclic Carbamates and Ureas via Hydrogen Atom Transfer and Radical-Polar Crossover

Guided by the transition-metal hydrogen atom transfer and radical-polar crossover concepts, we developed a functional-group-tolerant and scalable method for the synthesis of cyclic carbamates and ureas, which are found in the structures of bioactive compo

Method for synthesizing N - aryl oxazolidine -2 - ketone compound by ionic liquid catalysis

The invention discloses a method for catalytic synthesis of a N-aryloxazolane-2-one compound or a chiral N-aryloxazolane-2-one compound from an ionic liquid. The process of the preparation method is as follows: a catalytic amount of ionic liquid is added

Carbon dioxide-based facile synthesis of cyclic carbamates from amino alcohols

We report herein a straightforward general method for the synthesis of cyclic carbamates from amino alcohols and carbon dioxide in the presence of an external base and a hydroxyl group activating reagent. Utilizing p-toluenesulfonyl chloride (TsCl), the reaction proceeds under mild conditions, and the approach is fully applicable to the preparation of various high value-added 5- and 6-membered rings as well as bicyclic fused ring carbamates. DFT calculations and experimental results indicate a SN2-type reaction mechanism with high regio-, chemo-, and stereoselectivity.