183889-10-3

Basic information

• Product Name: 4,5-anhydro-2,3-O-isopropylidene-D-ribonic acid benzyl ester
• Synonyms: 4,5-anhydro-2,3-O-isopropylidene-D-ribonic acid benzyl ester
• CAS NO: 183889-10-3
• Molecular Weight: 278.305
• Mol File: 183889-10-3.mol

Chemical Properties

• CAS DataBase Reference: 4,5-anhydro-2,3-O-isopropylidene-D-ribonic acid benzyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 4,5-anhydro-2,3-O-isopropylidene-D-ribonic acid benzyl ester(183889-10-3)
• EPA Substance Registry System: 4,5-anhydro-2,3-O-isopropylidene-D-ribonic acid benzyl ester(183889-10-3)

Safety Data

• Hazardous Substances Data: 183889-10-3(Hazardous Substances Data)

Upstream product

• 40519-00-4 2,3-O-Isopropylidene-5-O-(p-tolylsulfonyl)-D-ribono-1,4-lactone 
• 100-51-6 benzyl alcohol 

Downstream Products

• 152006-17-2 2,3-O-isopropylidene-L-lyxono-1,4-lactone 

Relevant articles and documents

Synthesis of analogues of salacinol containing a carboxylate inner salt and their inhibitory activities against human maltase glucoamylase

The syntheses of analogues of the naturally occurring glycosidase inhibitor, salacinol, containing a carboxylate inner salt are described. Salacinol is a sulfonium ion with an internal sulfate counterion. The synthetic strategy relies on the nucleophilic

Stereoselective transformations leading to pentono -1, 4-lactones

The readily available 2, 3-O-isopropylidene-D-erythrose has been stereoselectively transformed into L-ribono and D/L lyxonolactone derivatives via dihydroxylation, iodolactonisation and epoxidation. Also D-ribono-1,4-lactone was converted into L-lyxono-1,