114743-31-6

Basic information

• Product Name: N⁶,O⁵'-bis(4,4'-dimethoxytrityl)-9-(3-deoxy-β-D-threo-pentofuranosyl)adenine
• Synonyms: N⁶,O⁵'-bis(4,4'-dimethoxytrityl)-9-(3-deoxy-β-D-threo-pentofuranosyl)adenine
• CAS NO: 114743-31-6
• Molecular Weight: 855.99
• Mol File: 114743-31-6.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: N⁶,O⁵'-bis(4,4'-dimethoxytrityl)-9-(3-deoxy-β-D-threo-pentofuranosyl)adenine(CAS DataBase Reference)
• NIST Chemistry Reference: N⁶,O⁵'-bis(4,4'-dimethoxytrityl)-9-(3-deoxy-β-D-threo-pentofuranosyl)adenine(114743-31-6)
• EPA Substance Registry System: N⁶,O⁵'-bis(4,4'-dimethoxytrityl)-9-(3-deoxy-β-D-threo-pentofuranosyl)adenine(114743-31-6)

Safety Data

• Hazardous Substances Data: 114743-31-6(Hazardous Substances Data)

Upstream product

• 118-00-3 G 
• 42822-80-0 2',3'-O-(dibutylstannylene)adenosine 
• 114765-61-6 N⁶,O⁵'-bis(4,4'-dimethoxytrityl)-3'-O-mesyl-2'-O-tosyladenosine 
• 109923-59-3 N⁶,O^5'-bis-(4,4'-dimethoxytrityl)-3'-O-tosyladenosine 
• 132625-21-9 2-N,5’-O-bis(4,4’-dimethoxytrityl)-gunaosine 
• 58-61-7 adenosine 
• 42776-78-3 2'-O-tosyladenosine 
• 109923-55-9 N⁶,O⁵'-bis(4,4'-dimethoxytrityl)-2'-O-tosyladenosine 
• 109923-58-2 3'-O-tosyladenosine tosylate salt 
• 124040-41-1 N⁶,O⁵'-bis(4,4'-dimethoxytrityl)adenosine 
• 40615-36-9 4,4'-dimethoxytrityl chloride 
• 124040-42-2 N⁶,O⁵'-bis(4,4'-dimethoxytrityl)-2',3'-di-O-mesyladenosine 
• 140679-70-5 2,2-Dimethyl-propionic acid (2R,3R,4R,5R)-5-[bis-(4-methoxy-phenyl)-phenyl-methoxymethyl]-2-(6-{[bis-(4-methoxy-phenyl)-phenyl-methyl]-amino}-purin-9-yl)-4-methanesulfonyloxy-tetrahydro-furan-3-yl ester 

Downstream Products

• 114743-30-5 N⁶,O^5'-bis(4,4'-dimethoxytrityl)-9-<(2R)-2-azido-2,3-dideoxy-β-D-glycero-pentofuranosyl>adenine 
• 114743-29-2 N⁶,O^5'-bis(4,4'-dimethoxytrityl)-9-(3-deoxy-2-O-mesyl-β-D-threo-pentofuranosyl)adenine 

Relevant articles and documents

General Method for the Synthesis of 2'-Azido-2',3'-dideoxynucleosides by the Use of -Hydride Shift and &β-Elimination Reactions

The title nucleoside (16U, C, G and H) were synthesized from pyrimidine and purine ribonucleosides in about 30percent overall yield in 6 steps via key intermediates, protected 3'-deoxy-arabino-nucleosides, which were obtained by deoxygenative -hydrid

The facile synthesis of 2'-azido-2',3'-dideoxyadenosine. Preparative applications of the deoxygenative [1,2]-hydride shift and β-elimination reactions of sulfonates with Mg(OMe)2-NaBH4

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