181259-63-2

Basic information

• Product Name: Adenosine, 5'-O-[(4-methoxyphenyl)diphenylmethyl]-N-(phenylmethyl)-
• CAS NO: 181259-63-2
• Molecular Formula: C37H35N5O5
• Molecular Weight: 629.715
• Mol File: 181259-63-2.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Adenosine, 5'-O-[(4-methoxyphenyl)diphenylmethyl]-N-(phenylmethyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Adenosine, 5'-O-[(4-methoxyphenyl)diphenylmethyl]-N-(phenylmethyl)-(181259-63-2)
• EPA Substance Registry System: Adenosine, 5'-O-[(4-methoxyphenyl)diphenylmethyl]-N-(phenylmethyl)-(181259-63-2)

Safety Data

• Hazardous Substances Data: 181259-63-2(Hazardous Substances Data)

Upstream product

• 4294-16-0 N₆-Benzyladenosine 
• 14470-28-1 mono-4-methoxytrityl chloride 

Downstream Products

• 181259-69-8 Benzoic acid (2R,3S,4R,5R)-5-(6-benzylamino-purin-9-yl)-4-hydroxy-2-[(4-methoxy-phenyl)-diphenyl-methoxymethyl]-tetrahydro-furan-3-yl ester 
• 181259-65-4 N⁶-benzyl-2',3'-di-O-benzoyl-5'-O-monomethoxytrityladenosine 
• 181259-73-4 Benzoic acid (2R,3R,4R,5R)-5-(6-benzylamino-purin-9-yl)-4-{(2-chloro-phenoxy)-[2-(4-nitro-phenyl)-ethoxy]-phosphoryloxy}-2-[(4-methoxy-phenyl)-diphenyl-methoxymethyl]-tetrahydro-furan-3-yl ester 
• 181259-75-6 Benzoic acid (2R,3R,4R,5R)-5-(6-benzylamino-purin-9-yl)-4-{hydroxy-[2-(4-nitro-phenyl)-ethoxy]-phosphoryloxy}-2-[(4-methoxy-phenyl)-diphenyl-methoxymethyl]-tetrahydro-furan-3-yl ester 

Relevant articles and documents

Preparation of (2?-5?)-oligonucleotides based on 6-N- benzylaminopurineriboside using the Spicaria violacea fungal enzyme complex

A method for chemico-enzymatic synthesis of (2?-5?)-oligonucleotides with 6-N-benzylaminopurineriboside as the nucleoside units was proposed. The method consisted of enzymatic hydrolysis of the oligonucleotides with mixed (2?-5?)-(3?-5?)-phosphodiesterbonds that were prepared by polymerization of 6-N-benzyladenosine-2?(3?)-monophosphate by using (3?-5?)-specific nuclease and phosphatase contained in the filtrate of culture medium of the mycelial fungus Spicaria violacea.

N6-benzyladenosine analogs of (A2′p)2A: Synthesis and activity to tobacco mosaic virus

Analogs of (2′-5′)oligoadenylate trimer with N6-benzyladenosine in various positions of the chain and the fully substituted trimer were synthesized by the phosphotriester method. The structures of compounds prepared were proved by UV, CD, and 1H NMR. The obtained substances inhibit replication of tobacco mosaic virus at a 10-8-10-6 M concentration, which is comparable with that of natural (A2′p)2A triadenylate.