1232680-29-3

Basic information

• Product Name: 7-((1S,5S)-5-methyl-4-oxocyclohex-2-enyloxy)-2H-chromen-2-one
• Synonyms: 7-((1S,5S)-5-methyl-4-oxocyclohex-2-enyloxy)-2H-chromen-2-one
• CAS NO: 1232680-29-3
• Molecular Weight: 270.285
• Mol File: 1232680-29-3.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 7-((1S,5S)-5-methyl-4-oxocyclohex-2-enyloxy)-2H-chromen-2-one(CAS DataBase Reference)
• NIST Chemistry Reference: 7-((1S,5S)-5-methyl-4-oxocyclohex-2-enyloxy)-2H-chromen-2-one(1232680-29-3)
• EPA Substance Registry System: 7-((1S,5S)-5-methyl-4-oxocyclohex-2-enyloxy)-2H-chromen-2-one(1232680-29-3)

Safety Data

• Hazardous Substances Data: 1232680-29-3(Hazardous Substances Data)

Upstream product

• 93-35-6 7-hydroxy-2H-chromen-2-one 
• 954390-26-2 tert-butyl (1S,5S)-5-methyl-4-oxocyclohex-2-enyl carbonate 

Relevant articles and documents

Synthesis of SL0101 carbasugar analogues: Carbasugars via Pd-catalyzed cyclitolization and post-cyclitolization transformations

A general approach to the stereoselective synthesis of 5a-carbasugars has been developed. The route mimics our palladium-catalyzed glycosylation/ postglycosylation approach to carbohydrates in that it also utilizes a highly regio- and stereospecific palladium-catalyzed allylation and postglycosylation reaction sequence for the installation of either d- or l-cyclitols. This cyclitolization/postcyclitolization sequence was used for the enantioselective synthesis of a cyclitol analogue of SL0101, its d-sugar enantiomer, as well as several acetylation pattern analogues.