124040-41-1

Basic information

• Product Name: 5'-O,N6-BIS-(4-METHOXYTRITYL)-ADENOSINE
• Synonyms: 5'-O,N6-BIS-(4-METHOXYTRITYL)-ADENOSINE;5''-O,N6-BIS-(4-METHOXYTRITAL)-ADENOSINE
• CAS NO: 124040-41-1
• Molecular Formula: C₅₂H₄₉N₅O₈
• Molecular Weight: 811.9222
• Mol File: 124040-41-1.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 5'-O,N6-BIS-(4-METHOXYTRITYL)-ADENOSINE(CAS DataBase Reference)
• NIST Chemistry Reference: 5'-O,N6-BIS-(4-METHOXYTRITYL)-ADENOSINE(124040-41-1)
• EPA Substance Registry System: 5'-O,N6-BIS-(4-METHOXYTRITYL)-ADENOSINE(124040-41-1)

Safety Data

• Hazardous Substances Data: 124040-41-1(Hazardous Substances Data)

Upstream product

• 40615-36-9 4,4'-dimethoxytrityl chloride 
• 58-61-7 adenosine 

Downstream Products

• 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 
• 114743-29-2 N⁶,O^5'-bis(4,4'-dimethoxytrityl)-9-(3-deoxy-2-O-mesyl-β-D-threo-pentofuranosyl)adenine 
• 114743-30-5 N⁶,O^5'-bis(4,4'-dimethoxytrityl)-9-<(2R)-2-azido-2,3-dideoxy-β-D-glycero-pentofuranosyl>adenine 
• 114743-31-6 N⁶,O⁵'-bis(4,4'-dimethoxytrityl)-9-(3-deoxy-β-D-threo-pentofuranosyl)adenine 
• 124040-42-2 N⁶,O⁵'-bis(4,4'-dimethoxytrityl)-2',3'-di-O-mesyladenosine 

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

SYNTHESIS OF 2'- AND 3'-AZIDO-2',3'-DIDEOXYADENOSINES. PREPARATIVE APPLICATIONS OF THE DEOXYGENATIVE-HYDRIDE SHIFT AND β-ELIMINATION REACTIONS OF O-SULFONYLATED ADENOSINES

2'-Azido-2',3'-dideoxyadenosine (9) has been synthesized from adenosine (1) in 6-8 steps.The key intermediate, N6,O5'-bis(4,4'-dimethoxytrityl)-9-(3-deoxy-β-D-threo-pentofuranosyl)adenine (6a), was prepared in a one-flask manner by t