245729-74-2

Basic information

• Product Name: benzyl 3,4-O-isopropylidene arabinoside
• Synonyms: benzyl 3,4-O-isopropylidene arabinoside
• CAS NO: 245729-74-2
• Molecular Weight: 280.321
• Mol File: 245729-74-2.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: benzyl 3,4-O-isopropylidene arabinoside(CAS DataBase Reference)
• NIST Chemistry Reference: benzyl 3,4-O-isopropylidene arabinoside(245729-74-2)
• EPA Substance Registry System: benzyl 3,4-O-isopropylidene arabinoside(245729-74-2)

Safety Data

• Hazardous Substances Data: 245729-74-2(Hazardous Substances Data)

Upstream product

• 100-51-6 benzyl alcohol 
• 87-72-9 L-(+)-arabinose 
• 250224-22-7 (3R,4S,5S)-2-Benzyloxy-tetrahydro-pyran-3,4,5-triol 
• 77-76-9 2,2-dimethoxy-propane 
• 67-64-1 acetone 

Downstream Products

• 118533-09-8 [(3aS,7aR)-6-Benzyloxy-2,2-dimethyl-dihydro-[1,3]dioxolo[4,5-c]pyran-(7E)-ylidene]-acetic acid methyl ester 
• 118533-09-8 [(3aS,7aR)-6-Benzyloxy-2,2-dimethyl-dihydro-[1,3]dioxolo[4,5-c]pyran-(7E)-ylidene]-acetic acid methyl ester 
• 118533-10-1 (7S,7aR)-4-Benzyloxy-7-hydroxy-7,7a-dihydro-4H,6H-furo[3,2-c]pyran-2-one 
• 28070-06-6 (3aS,7aS)-6-Benzyloxy-2,2-dimethyl-dihydro-[1,3]dioxolo[4,5-c]pyran-7-one 

Relevant articles and documents

Synthesis and in vitro evaluation of novel highly potent coumarin inhibitors of gyrase B

The design, synthesis, and in vitro biological activity of a series of novel coumarin inhibitors of gyrase B is presented. Replacement of the 3- acylamino residue (3-NHCOR) of coumarin drags with reversed isosteres C(=O)R, C(=N-OR)R', COOR, CONHR and CONH

A CONCISE SYNTHESIS OF PATULIN FROM ARABINOSE

Conversion of arabinose (5) to the protected ketone (7), followed by Wittig condensation to (9), acid catalysed cyclisation (to 10), and dehydration, provides a brief synthesis of the fungal metabolite patulin (1), produced by Penicillium and Aspergilius