85315-74-8

Basic information

• Product Name: 3-C-(benzyloxymethyl)-3,5,6-trideoxy-1,2-O-isopropylidene-α-D-ribo-5-hexenofuranose
• Synonyms: 3-C-(benzyloxymethyl)-3,5,6-trideoxy-1,2-O-isopropylidene-α-D-ribo-5-hexenofuranose
• CAS NO: 85315-74-8
• Molecular Weight: 290.359
• Mol File: 85315-74-8.mol

Chemical Properties

• CAS DataBase Reference: 3-C-(benzyloxymethyl)-3,5,6-trideoxy-1,2-O-isopropylidene-α-D-ribo-5-hexenofuranose(CAS DataBase Reference)
• NIST Chemistry Reference: 3-C-(benzyloxymethyl)-3,5,6-trideoxy-1,2-O-isopropylidene-α-D-ribo-5-hexenofuranose(85315-74-8)
• EPA Substance Registry System: 3-C-(benzyloxymethyl)-3,5,6-trideoxy-1,2-O-isopropylidene-α-D-ribo-5-hexenofuranose(85315-74-8)

Safety Data

• Hazardous Substances Data: 85315-74-8(Hazardous Substances Data)

Upstream product

• 2280-44-6 D-Glucose 
• 620630-82-2 1,2 5,6-O-di(isopropylidene)-α-D-allofuranose 
• 21665-16-7 3-deoxy-1,2:5,6-di-O-isopropylidene-3-C-methylene-α-D-ribo-hexofuranose 
• 100-39-0 benzyl bromide 
• 582-52-5 1,2:5,6-di-O-isopropylidene-α-D-glucofuranose 
• 85315-68-0 3-C-(benzyloxymethyl)-3-deoxy-1,2-O-isopropylidene-α-D-allofuranose 
• 2847-00-9 1,2:5,6-di-O-isopropylidene-α-D-hexofuran-3-ulose 
• 21665-16-7 O¹,O²;O⁵,O⁶-diisopropylidene-3-methylene-α-D-ribo-3-deoxy-hexofuranose 
• 69832-48-0 ((3aR,5S,6R,6aR)-tetrahydro-2,2-dimethyl-5-((R)-2,2-dimethyl-1,3-dioxolan-4-yl)furo[2,3-d][1,3]dioxol-6-yl)methanol 
• 2847-00-9 1,2:5,6-di-O-isopropylidene-α-D-ribo-3-hexulofuranose 
• 69832-48-0 3-C-deoxy-3-C-hydroxymethyl-1,2;5,6-di-O-isopropylidene-α-D-allo-furanose 
• 314061-33-1 Methanesulfonic acid (R)-1-((3aR,5S,6R,6aR)-6-benzyloxymethyl-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-yl)-2-methanesulfonyloxy-ethyl ester 
• 85315-67-9 3-C-(benzyloxymethyl)-3-deoxy-1,2:5,6-di-O-isopropylidene-α-D-allofuranose 

Downstream Products

• 153337-07-6 (1S,2R,3S)-2-vinyl-3-(benzyloxymethyl)cyclobutanol 
• 934279-75-1 3-benzyloxy-4-benzyloxymethyl-5-vinyl-dihydro-furan-2-one 
• 934279-78-4 methyl-2-C-benzyloxy-3-deoxy-3-C-benzyloxymethyl-5-methylene-ribo-hexofuranoside 
• 314061-35-3 2-((3aR,5R,6R,6aR)-6-Benzyloxymethyl-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-yl)-ethanol 

Relevant articles and documents

Towards the enantioselective synthesis of anti-HIV agents litseaverticillols C and K from d-glucose

The first enantioselective synthesis towards the litseaverticillols C and K has been achieved, from d-glucose, using the ring closing metathesis (RCM) and Wittig reactions as key steps.

Synthesis of a phosphinic acid analogue of cyclic AMP

Synthesis of a cyclic phosphinate ester analogue of cyclic AMP was achieved by using a double Arbuzov-type cyclisation of bis-trimethylsilyl phosphonite onto a sugar dihalide derivative as the key step. (C) 2000 Elsevier Science Ltd.