64520-63-4

Basic information

• Product Name: 2,3,4,5-tetra-O-benzyl diethyl dithioacetal D-arabinose
• Synonyms: 2,3,4,5-tetra-O-benzyl diethyl dithioacetal D-arabinose
• CAS NO: 64520-63-4
• Molecular Weight: 616.886
• Mol File: 64520-63-4.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 2,3,4,5-tetra-O-benzyl diethyl dithioacetal D-arabinose(CAS DataBase Reference)
• NIST Chemistry Reference: 2,3,4,5-tetra-O-benzyl diethyl dithioacetal D-arabinose(64520-63-4)
• EPA Substance Registry System: 2,3,4,5-tetra-O-benzyl diethyl dithioacetal D-arabinose(64520-63-4)

Safety Data

• Hazardous Substances Data: 64520-63-4(Hazardous Substances Data)

Upstream product

• 10323-20-3 D-Arabinose 
• 28697-53-2 D-arabinopyranose 
• 1941-50-0 D-arabinose diethyl dithioacetal 
• 100-39-0 benzyl bromide 

Downstream Products

• 14233-64-8 tri-O-benzyl-D-arabinolactone 
• 216772-75-7 2,3,4,5-tetra-O-benzyl-N-<2,2-bis(diethoxyphosphinyl)ethyl>-D-arabinonamide 
• 216772-31-5 2,3,4,5-tetra-O-benzyl-N-methyl-D-arabinonamide 
• 216772-27-9 2,3,4,5-tetra-O-benzyl-N-<2-(benzyloxy)-2-oxoethyl>-D-arabinonamide 
• 216772-52-0 2,3,4,5-tetra-O-benzyl-N-(2-bromoethyl)-D-arabinonamide 
• 216772-11-1 2,3,4,5-tetra-O-benzyl-D-arabinonamide 
• 116087-65-1 (2S,3R,4R)-2,3,4,5-tetrakis(benzyloxy)pentanal 

Relevant articles and documents

Regioselective Synthesis of Difluorinated C-Furanosides Involving a Debenzylative Cycloetherification

A highly regioselective synthesis of valuable gem-difluorinated C-furanosides from unprotected aldoses via a debenzylative cycloetherification (DBCE) reaction induced by diethylaminosulfur trifluoride is descibed. The scope and limitations of this DBCE reaction are described using a series of commercially available pentoses and hexoses to afford, without selective protection/deprotection sequences, the corresponding gem-difluorinated C-furanosides in moderate to good yields.

N-Monoalkylation of Tetra-O-benzyl-D-arabinonamide: Synthesis of Some Open-Chain Analogues of N-Acetylneuraminic Acid and Their Evaluation as Sialidase Inhibitors

N-Arabinonoylglycine 2, its phospho analogue (arabinonoylamino)methylphosphonate 14, N-arabinonoyltaurine salt 18, and [2-(arabinonoylamino)ethylidene]bis[phosphonic acid] 22 have been synthesized from D-arabinose in seven (2 or 14), and eight steps (18 o