114861-24-4

Basic information

• Product Name: 3-deoxy-1,2-O-(1-methylethylidene)-5-O-(phenylmethyl)-α-L-xylofuranose
• Synonyms: 3-deoxy-1,2-O-(1-methylethylidene)-5-O-(phenylmethyl)-α-L-xylofuranose
• CAS NO: 114861-24-4
• Molecular Weight: 264.321
• Mol File: 114861-24-4.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 3-deoxy-1,2-O-(1-methylethylidene)-5-O-(phenylmethyl)-α-L-xylofuranose(CAS DataBase Reference)
• NIST Chemistry Reference: 3-deoxy-1,2-O-(1-methylethylidene)-5-O-(phenylmethyl)-α-L-xylofuranose(114861-24-4)
• EPA Substance Registry System: 3-deoxy-1,2-O-(1-methylethylidene)-5-O-(phenylmethyl)-α-L-xylofuranose(114861-24-4)

Safety Data

• Hazardous Substances Data: 114861-24-4(Hazardous Substances Data)

Upstream product

• 38166-60-8 1,2:5,6-di-O-isopropylidene-α-L-glucofuranoside 
• 100638-80-0 1,2:5,6-di-O-isopropylidene-3-O-(methylthio)thiocarbonyl-β-D-idose 
• 4613-68-7 (3aS,5R,6aS)-2,2-Dimethyl-tetrahydro-furo[2,3-d][1,3]dioxole-5-carbaldehyde 
• 4005-46-3 3-deoxy-1,2-O-isopropylidene-α-L-glucose 
• 32785-98-1 3-deoxy-1,2:5,6-di-O-isopropylidene-β-D-lyxo-hexose 
• 41546-31-0 L-xylose 
• 114861-22-2 1,2-O-isopropylidene-α-L-xylofuranose 
• 114861-15-3 Thiocarbonic acid O-[(3aS,5S,6R,6aS)-5-(tert-butyl-diphenyl-silanyloxymethyl)-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-6-yl] ester O-phenyl ester 
• 220827-73-6 5-O-tert-butyldiphenylsilyl-1,2-O-isopropylidene-α-L-xylofuranose 
• 106799-16-0 tert-Butyl-((3aS,5R,6aS)-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-ylmethoxy)-diphenyl-silane 
• 100-39-0 benzyl bromide 
• 114861-23-3 3-deoxy-1,2-O-isopropylidene-α-L-erythro-pentofuranose 

Downstream Products

• 133804-87-2 (3'R,5'R)-2-amino-1,9-dihydro-9-<5'-(hydroxymethyl)tetrahydrofuran-3'-yl>-6H-purin-6-one 
• 142941-44-4 (3'R,5'R)-9-<5'-<(benzyloxy)methyl>tetrahydrofuran-3'-yl>-6-chloro-9H-purin-2-amine 
• 142941-43-3 (3'R,5'R)-9-<5'-<(benzyloxy)methyl>tetrahydrofuran-3'-yl>9H-purin-6-amine 
• 142941-42-2 (3'R,5'R)-1-<5'-<(benzyloxy)methyl>tetrahydrofuran-3'-yl>-5-methylpyrimidine-2,4(1H,3H)-dione 
• 132813-68-4 (3'R,5'R)-1-<5'-<(benzyloxy)methyl>tetrahydrofuran-3'-yl>-pyrimidine-2,4(1H,3H)-dione 
• 132813-69-5 (3'R,5'R)-4-amino-1-<5'-<(benzyloxy)methyl>tetrahydrofuran-3'-yl>-5-methylpyrimidine-2(1H)-one 
• 142941-41-1 (2R,4S)-2-<(benzyloxy)methyl>-4-<(methylsulfonyl)oxy>tetrahydrofuran 
• 78038-33-2 3S,5R-5-<(benzyloxy)methyl>tetrahydrofuran-3-ol 
• 127682-75-1 IsoddA 
• 106799-18-2 3,5-dideoxy-6-O-<(1,1-dimethylethyl)dimethylsilyl>-2,4-O-(1-methylethylidene)-1-O-(phenylmethyl)-D-erythro-hexitol 
• 114925-53-0 3,5-dideoxy-2,4-O-(1-methylethylidene)-1-O-(phenylmethyl)-D-erythro-hexitol 
• 106799-17-1 (2R,4S)-1-<(phenylmethoxy)methyl>5-hexene-2,4-diol 
• 114925-52-9 <4R-(4α,5α)>-4-<(phenylmethoxy)methyl>-6-ethenyl-2,2-dimethyl-1,3-dioxane 
• 114861-37-9 3-deoxy-5-O-(phenylmethyl)-α-L-xylofuranose 

Relevant articles and documents

Enantiospecific Synthesis of 3'-Hetero-dideoxy Nucleoside Analogues as Potential Anti-HIV Agents

Two series of analogues of 2',3'-dideoxy carbocyclic nucleosides, in which the 3'-carbon atom is replaced by either an oxygen or a sulfur atom, have been prepared enantiospecifically from diacetone-L-glucose and diacetone-D-glucose respectively.Within eac

Stereocontrolled Construction of Key Building Blocks for the Total Synthesis of Amphoteronolide B and Amphotericin B

-