105454-46-4

Basic information

• Product Name: methyl 2-deoxy-5-O-trityl-α,β-D-erythro-pentofuranoside
• Synonyms: methyl 2-deoxy-5-O-trityl-α,β-D-erythro-pentofuranoside
• CAS NO: 105454-46-4
• Molecular Weight: 390.479
• Mol File: 105454-46-4.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: methyl 2-deoxy-5-O-trityl-α,β-D-erythro-pentofuranoside(CAS DataBase Reference)
• NIST Chemistry Reference: methyl 2-deoxy-5-O-trityl-α,β-D-erythro-pentofuranoside(105454-46-4)
• EPA Substance Registry System: methyl 2-deoxy-5-O-trityl-α,β-D-erythro-pentofuranoside(105454-46-4)

Safety Data

• Hazardous Substances Data: 105454-46-4(Hazardous Substances Data)

Upstream product

• 114071-58-8 methyl 3,5-O-isopropylidene-2-O-<(methylthio)-thiocarbonyl>-αβ-D-xylofuranoside 
• 116195-62-1 methyl 2-deoxy-3,5-O-isopropylidene-αβ-D-threo-pentofuranoside 
• 112245-59-7 methyl 3,5-O-isopropylidene-αβ-D-xylofuranoside 
• 76-83-5 trityl chloride 
• 51255-17-5 1-O-methyl-2-deoxy-D-ribofuranoside 
• 863396-37-6 methyl 2-deoxy-αβ-D-threo-pentofuranoside 

Downstream Products

• 105454-48-6 3-O-Benzyl-2-deoxy-5-(triphenylmethyl)-D-erythro-pentofuranoside 
• 113666-59-4 methyl 2-deoxy-3-O-hexadecyl-5-O-trityl-α,β-D-erythro-pentofuranoside 
• 532413-72-2 methyl 3-azido-2,3-dideoxy-5-O-triphenylmethyl-D-erythro-pentofuranoside 
• 1053649-22-1 1-<2-deoxy-3-O-<2-(formamido)ethyl>-5-O-trityl-α-D-erythro-pentofuranosyl>-5-nitrouracil 
• 1053267-66-5 1-<2-deoxy-3-O-<2-(formamido)ethyl>-5-O-trityl-α-D-erythro-pentofuranosyl>uracil 
• 401586-01-4 2,2-Dimethyl-propionic acid (2R,3S)-2-(2,2-dimethyl-propionyloxymethyl)-5-phenylselanyl-tetrahydro-furan-3-yl ester 
• 659720-30-6 (2R,3S)-2-Hydroxymethyl-5-phenylselanyl-tetrahydro-furan-3-ol 
• 116390-97-7 Methanesulfonic acid (2R,3R)-5-methoxy-2-trityloxymethyl-tetrahydro-furan-3-yl ester 

Relevant articles and documents

Enantiospecific synthesis of the heparanase inhibitor (+)-trachyspic acid and stereoisomers from a common precursor

The total synthesis of natural (+)-trachyspic acid and its enantiomer is described starting from a common 2-deoxy-d-ribose derivative. The synthesis of the corresponding C3 epimers from the same starting material is also described. Each stereoisomer was a

2-deoxyuridines and riboside precursors

A process is provided for the preparation of certain 2-deoxyuridines including the steps forming a substituted alkyl 5-O-"protected"-2-deoxyribofuranoside, hydrocarbylating the latter compound, and condensing the hydrocarbylated compound in the presence o