1203507-23-6

Basic information

• Product Name: 4-methoxyphenyl (R)-4-isopropyl-2-(4-methoxyphenyl)-5-oxo-4,5-dihydrooxazole-4-carboxylate
• Synonyms: 4-methoxyphenyl (R)-4-isopropyl-2-(4-methoxyphenyl)-5-oxo-4,5-dihydrooxazole-4-carboxylate
• CAS NO: 1203507-23-6
• Molecular Weight: 383.401
• Mol File: 1203507-23-6.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 4-methoxyphenyl (R)-4-isopropyl-2-(4-methoxyphenyl)-5-oxo-4,5-dihydrooxazole-4-carboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: 4-methoxyphenyl (R)-4-isopropyl-2-(4-methoxyphenyl)-5-oxo-4,5-dihydrooxazole-4-carboxylate(1203507-23-6)
• EPA Substance Registry System: 4-methoxyphenyl (R)-4-isopropyl-2-(4-methoxyphenyl)-5-oxo-4,5-dihydrooxazole-4-carboxylate(1203507-23-6)

Safety Data

• Hazardous Substances Data: 1203507-23-6(Hazardous Substances Data)

Upstream product

• 1203507-22-5 4-methoxyphenyl 2-(4-methoxyphenyl)-4-isopropyloxazol-5-yl carbonate 

Relevant articles and documents

Isothiourea-mediated asymmetric O- to C-carboxyl transfer of oxazolyl carbonates: Structure-selectivity profiles and mechanistic studies

The structural motif within a series of tetrahydropyrimidine-based isothioureas necessary for generating high asymmetric induction in the asymmetric Steglich rearrangement of oxazolyl carbonates is fully explored, with crossover and dynamic 19F NMR experiments used to develop a mechanistic understanding of this transformation. Copyright