1620809-10-0

Basic information

• Product Name: C₂₄H₃₁NO₁₂
• CAS NO: 1620809-10-0
• Molecular Weight: 525.51
• Mol File: 1620809-10-0.mol

Chemical Properties

• CAS DataBase Reference: C₂₄H₃₁NO₁₂(CAS DataBase Reference)
• NIST Chemistry Reference: C₂₄H₃₁NO₁₂(1620809-10-0)
• EPA Substance Registry System: C₂₄H₃₁NO₁₂(1620809-10-0)

Safety Data

• Hazardous Substances Data: 1620809-10-0(Hazardous Substances Data)

Upstream product

• 1620809-05-3 C₁₇H₂₁NO₅ 
• 1620809-03-1 (R)-1-[(2R,3R)-3-acetoxy-1-(benzyloxycarbonyl)-5-vinyl-1,2,3,6-tetrahydropyridin-2-yl]ethane-1,2-diyl diacetate 
• 1620809-02-0 C₂₀H₂₃NO₅ 
• 910479-44-6 ((3aR,5R,6R,6aR)-2,2-Dimethyl-5-vinyl-tetrahydro-furo[2,3-d][1,3]dioxol-6-yl)-carbamic acid benzyl ester 
• 1620809-08-6 C₂₂H₂₅NO₉ 
• 1620809-01-9 benzyl (3aR,5R,6R,6aR)-2,2-dimethyl-5-vinyltetrahydrofuro[2,3-d][1,3]dioxol-6-yl(prop-2-ynyl)carbamate 
• 1620809-07-5 (R)-1-[(2R,3R)-3-acetoxy-5-(acetoxymethyl)-1-(benzyloxycarbonyl)-1,2,3,6-tetrahydropyridin-2-yl]ethane-1,2-diyl diacetate 
• 1620809-06-4 (R)-1-[(2R,3R)-3-acetoxy-1-(benzyloxycarbonyl)-5-(1,2-dihydroxyethyl)-1,2,3,6-tetrahydropyridin-2-yl]ethane-1,2-diyl diacetate 

Downstream Products

• 1620809-09-7 (2S,3S,4S,5S)-5-(acetoxymethyl)-1-(benzyloxycarbonyl)-2-[(R)-1,2-bis(acetoxyethyl)]piperidine-3,4,5-triyl triacetate 

Relevant articles and documents

Synthesis and glycosidase inhibition study of 2-C-hydroxymethyl- and 6-C-hydroxymethyl-branched piperidines from D-glucose using ene-yne metathesis as a key step

Two polyhydroxylated piperidine-based 2-C-hydroxymethyl-branched analogues of L-1-deoxyallonojirimycin (L-allo-DNJ) were synthesized from readily available 1,2:5,6-di-O-isopropylidene-α-glucofuranose through an ene-yne metathesis as the key step. The glycosidase inhibition activity of these compounds against some commercially available enzymes was examined, and the analogues were found to be very selective glycosidase inhibitors at concentrations in the range of 21-44 μM. Piperidine-based 2-C-hydroxymethyl-branched analogues of L-1-deoxyallonojirimycin (L-allo-DNJ) were synthesized from readily available D-glucose by using an ene-yne metathesis as the key step; PG = protecting group. The glycosidase inhibition activity of these compounds was studied and found to be active and very selective. Copyright