1312808-04-0

Basic information

• Product Name: 2-(4-methoxyphenyl)-4-methyloxazol-5-yl naphthalen-1-yl carbonate
• Synonyms: 2-(4-methoxyphenyl)-4-methyloxazol-5-yl naphthalen-1-yl carbonate
• CAS NO: 1312808-04-0
• Molecular Weight: 375.381
• Mol File: 1312808-04-0.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 2-(4-methoxyphenyl)-4-methyloxazol-5-yl naphthalen-1-yl carbonate(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(4-methoxyphenyl)-4-methyloxazol-5-yl naphthalen-1-yl carbonate(1312808-04-0)
• EPA Substance Registry System: 2-(4-methoxyphenyl)-4-methyloxazol-5-yl naphthalen-1-yl carbonate(1312808-04-0)

Safety Data

• Hazardous Substances Data: 1312808-04-0(Hazardous Substances Data)

Upstream product

• 99553-79-4 2-(4-methoxyphenyl)-4-methyl-5-oxo-4,5-dihydrooxazole 
• 3759-61-3 1-naphthyl chloroformate 

Downstream Products

• 1312807-97-8 4-benzyl-2-(4-methoxyphenyl)oxazol-5-yl naphthalen-1-yl carbonate 
• 1318802-51-5 naphthalen-1-yl 2-(4-methoxyphenyl)-4-methyl-5-oxo-4,5-dihydrooxazole-4-carboxylate 
• 1318802-52-6 naphthalen-1-yl 4-benzyl-2-(4-methoxyphenyl)-5-oxo-4,5-dihydrooxazole-4-carboxylate 
• 627877-63-8 2-(4-methoxyphenyl)-4-methyloxazol-5-yl phenyl carbonate 
• 1312808-05-1 naphthalen-1-yl 2-(4-methoxyphenyl)-4-methyl-5-oxo-4,5-dihydrooxazole-4-carboxylate 

Relevant articles and documents

Organic base effects in NHC promoted O- to C-carboxyl transfer; Chemoselectivity profiles, mechanistic studies and domino catalysis

The O- to C-carboxyl transfer of oxazolyl carbonates promoted by triazolinylidenes, generated in situ with NEt3, shows a markedly different rate and chemoselectivity profile to the same reaction promoted by triazolinylidenes generated using KHM