1531624-35-7

Basic information

• Product Name: (R)-phenyl 3,6-dimethyl-2-oxo-2,3-dihydrobenzofuran-3-carboxylate
• Synonyms: (R)-phenyl 3,6-dimethyl-2-oxo-2,3-dihydrobenzofuran-3-carboxylate
• CAS NO: 1531624-35-7
• Molecular Weight: 282.296
• Mol File: 1531624-35-7.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: (R)-phenyl 3,6-dimethyl-2-oxo-2,3-dihydrobenzofuran-3-carboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: (R)-phenyl 3,6-dimethyl-2-oxo-2,3-dihydrobenzofuran-3-carboxylate(1531624-35-7)
• EPA Substance Registry System: (R)-phenyl 3,6-dimethyl-2-oxo-2,3-dihydrobenzofuran-3-carboxylate(1531624-35-7)

Safety Data

• Hazardous Substances Data: 1531624-35-7(Hazardous Substances Data)

Upstream product

• 1885-14-9 phenyl chloroformate 
• 65817-24-5 3,6-dimethyl-3H-benzo[b]furan-2-one 
• 1531624-14-2 3,6-dimethylbenzofuran-2-yl phenyl carbonate 

Relevant articles and documents

3- season carbon chiral -C-acyl Phthalidyl derivative and its preparation method

The invention discloses a 3-quaternary carbon chiral-C-acylbenzofuranone derivative and a preparation method thereof. O-acylbenzofuranone derivative as a raw material undergoes an asymmetric Black rearrangement reaction in the presence of a chiral imidazole catalyst to produce the 3-quaternary carbon chiral-C-acylbenzofuranone derivative. The preparation method utilizes a cheap and easily available chiral nucleophilic catalyst to replace an expensive catalyst used in the prior art, has mild catalytic reaction conditions and simple processes, and has a good yield and enantioselectivity. Through further derivation, the obtained 3-quaternary carbon chiral-C-acylbenzofuranone derivative can be used for synthesis of a physiologically active molecule.