14233-64-8

Basic information

• Product Name: 3β,4α-Bis(benzyloxy)-5β-(benzyloxymethyl)tetrahydrofuran-2-one
• Synonyms: 2-O,3-O,5-O-Tribenzyl-D-arabinoic acid 1,4-lactone;2-O,3-O,5-O-Tribenzyl-D-arabinoic acid γ-lactone;3β,4α-Bis(benzyloxy)-5β-(benzyloxymethyl)-4,5-dihydrofuran-2(3H)-one;3β,4α-Bis(benzyloxy)-5β-(benzyloxymethyl)tetrahydrofuran-2-one;2,3,5-tri-O-benzyl-D-arabino-γ-lactone;2,3,5-Tris-O-(phenylmethyl)-D-arabinonic acid gamma-lactone
• CAS NO: 14233-64-8
• Molecular Formula: C₂₆H₂₆O₅
• Molecular Weight: 418.48164
• Mol File: 14233-64-8.mol
• Article Data: 39

Chemical Properties

• Melting Point: 70-70.5 °C(Solv: ligroine (8032-32-4); ethyl acetate (141-78-6))
• Boiling Point: 576.8±50.0 °C(Predicted)
• Appearance: /
• Density: 1.21±0.1 g/cm3(Predicted)
• CAS DataBase Reference: 3β,4α-Bis(benzyloxy)-5β-(benzyloxymethyl)tetrahydrofuran-2-one(CAS DataBase Reference)
• NIST Chemistry Reference: 3β,4α-Bis(benzyloxy)-5β-(benzyloxymethyl)tetrahydrofuran-2-one(14233-64-8)
• EPA Substance Registry System: 3β,4α-Bis(benzyloxy)-5β-(benzyloxymethyl)tetrahydrofuran-2-one(14233-64-8)

Safety Data

• Hazardous Substances Data: 14233-64-8(Hazardous Substances Data)

Upstream product

• 81927-55-1 O-benzyl 2,2,2-trichloroacetimidate 
• 5336-08-3 D-Ribono-1,4-lactone 
• 79875-99-3 (2R,3R,4R)-2,3,4,5-tetrakis(benzyloxy)pentanal 
• 50615-49-1 2,3,4,5-tetra-O-benzyl diethyl dithioacetal D-ribose 
• 10257-32-6 D-ribose 
• 7152-47-8 D-ribose diethyl dithioacetal 
• 532-20-7 D-Ribose 
• 100-39-0 benzyl bromide 
• 144950-24-3 2,3,5-tri-O-benzyl-D-arabinofuranose 
• 620946-81-8 (Z)-2,3,5-tri-O-benzyl-D-ribonhydroximo-1,4-lactone 
• 620946-65-8 (Z)-2,3,5-tri-O-benzyl-D-ribose oxime 
• 16838-89-4 2,3,5-tri-O-benzyl-D-ribofuranose 
• 39085-59-1 trisylhydrazine 
• 89361-52-4 2,3,5-tris-O-(phenylmethyl)-β-D-ribofuranose 

Downstream Products

• 853260-31-8 ((2R,3R,4R,5R)-3,4-Bis-benzyloxy-5-benzyloxymethyl-tetrahydro-furan-2-ylethynyl)-trimethyl-silane 
• 853260-33-0 C₅₄H₅₄O₈ 
• 163580-29-8 3,6-anhydro-4,5,7-tri-O-benzyl-1,1,2,2-tetradehydro-1,2-dideoxy-D-manno-heptitol 
• 354113-40-9 (3R,4R,5R)-3,4-Bis-benzyloxy-5-benzyloxymethyl-2-(3,5,6-tris-phenylsulfanyl-pyrazin-2-yl)-tetrahydro-furan-2-ol 
• 354113-39-6 (3R,4R,5R)-3,4-Bis-benzyloxy-5-benzyloxymethyl-2-(3,5-dichloro-6-iodo-pyrazin-2-yl)-tetrahydro-furan-2-ol 
• 377777-50-9 5-((2S,3S,4R,5R)-3,4-Bis-benzyloxy-5-benzyloxymethyl-tetrahydro-furan-2-yl)-[2,2']bipyridinyl 
• 134001-24-4 (3R,4R,5S)-5-[(benzyloxy)methyl]-3,4-bis(phenoxymethyl)dihydrofuran-2(3H)-one 
• 229638-10-2 C₄₆H₄₂N₂O₇ 
• 190907-81-4 2-amino-3-methyl-5-(2',3,',5'-tri-O-benzyl-β-D-ribofuranosyl)pyridine 
• 183311-61-7 2-amino-5-(2',3,',5'-tri-O-benzyl-β-D-ribofuranosyl)pyridine 
• 181582-01-4 (3R,4R,5R)-3,4-Bis-benzyloxy-2-(3-benzyloxy-5-chloro-pyrazin-2-yl)-5-benzyloxymethyl-tetrahydro-furan-2-ol 

Relevant articles and documents

Stereoselective Palladium-Catalyzed Arylation of Exo-Glycals with Aryl Iodides

A novel methodology for the arylation of exo-glycals has been developed. A range of exo-glycals underwent reactions with aryl iodides in the presence of a palladium catalyst. The transformation proceeded in a stereoselective manner to afford Z-isomers. Th

Compound for treating viral infection and preparation method and application of compound

The invention provides a preparation for treating viral infection and pneumovirus subfamily viral infection, a method, a compound as shown in a formula (I) and a method and intermediate for synthesis of the compound as shown in the formula (I).

Novel compound and application thereof

The invention relates to a novel compound and application thereof, and also relates to an application of the compound in preparation of antiviral drugs and the like. In particular, AIDS virus is present. Application of hepatitis B virus, paramyxovirus and