944476-43-1

Basic information

• Product Name: C₂₄H₂₀N₂O₇
• Synonyms: C₂₄H₂₀N₂O₇
• CAS NO: 944476-43-1
• Molecular Weight: 448.432
• Mol File: 944476-43-1.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: C₂₄H₂₀N₂O₇(CAS DataBase Reference)
• NIST Chemistry Reference: C₂₄H₂₀N₂O₇(944476-43-1)
• EPA Substance Registry System: C₂₄H₂₀N₂O₇(944476-43-1)

Safety Data

• Hazardous Substances Data: 944476-43-1(Hazardous Substances Data)

Upstream product

• 944476-40-8 (2R,3R,3aS,9aR)-3-hydroxy-2-(hydroxymethyl)-3a-methyl-2,3,3a,9a-tetrahydro-6H-furo[2',3':4,5]oxazolo[3,2-a]pyrimidin-6-one 
• 98-88-4 benzoyl chloride 
• 922-67-8 propynoic acid methyl ester 
• 58-96-8 uridine 
• 23643-36-9 2′,3′,5′-tri-O-benzoyl-2′-C-methyluridine 
• 7392-74-7 (3R,4R,5R)-5-((benzoyloxy)methyl)-3-methyl-2-oxotetrahydrofuran-3,4-diyl dibenzoate 
• 492-30-8 2-C-methyl-D-ribono-1,4-lactone 
• 944476-44-2 C₂₄H₂₂N₂O₈ 
• 54618-11-0 3’,5’-dibenzoyluridine 
• 31616-01-0 3’,5’-O-benzoyl-2,2’-anhydrouridine 

Downstream Products

• 944476-44-2 C₂₄H₂₂N₂O₈ 
• 944476-44-2 ((2R,3R,4S,5R)-3-(benzoyloxy)-5-(2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)-4-hydroxy-4-methyltetrahydrofuran-2-yl)methyl benzoate 
• 863329-66-2 2'-deoxy-2'-fluoro-2'-methyluridine 
• 863329-65-1 (2‘R)-2‘-deoxy-2’-fluoro-2-methyluridine-3’,5’-dibenzoate 

Relevant articles and documents

A (2 'R) -2' - deoxy -2 '- fluoro -2' - methyl urea glucoside preparation method (by machine translation)

The invention discloses a (2 'R) -2' - deoxy -2 '- fluoro -2' - methyl urea glucoside (type I) synthetic method. Cheap and easily available starting material, through the hydroxyl protection, cyclization, the links such as fluoride, obtains the type I compound. (by machine translation)

Anomeric stereospecific synthesis of 2′-C-methyl β-nucleosides; the Holy reaction of cyanamide with 2-C-methyl-d-arabinose

The sequential reactions of 2-C-methyl-d-arabinose with cyanamide and methyl propiolate afford an anhydronucleoside, which may be opened under acid conditions with inversion at C2′, to give 2′-C-methyl uridine; ring opening with sodium hydroxide gave 2′-C