93135-69-4

Basic information

• Product Name: Adenosine, N-benzoyl-2',3'-O-(1-methylethylidene)-, 5'-benzoate
• CAS NO: 93135-69-4
• Molecular Formula: C27H25N5O6
• Molecular Weight: 515.525
• Mol File: 93135-69-4.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Adenosine, N-benzoyl-2',3'-O-(1-methylethylidene)-, 5'-benzoate(CAS DataBase Reference)
• NIST Chemistry Reference: Adenosine, N-benzoyl-2',3'-O-(1-methylethylidene)-, 5'-benzoate(93135-69-4)
• EPA Substance Registry System: Adenosine, N-benzoyl-2',3'-O-(1-methylethylidene)-, 5'-benzoate(93135-69-4)

Safety Data

• Hazardous Substances Data: 93135-69-4(Hazardous Substances Data)

Upstream product

• 362-75-4 2',3'-isopropylidene adenosine 
• 93-97-0 benzoic acid anhydride 
• 58-61-7 adenosine 
• 98-88-4 benzoyl chloride 

Downstream Products

• 39947-04-1 N-6-benzoyl-2',3'-O-isopropylideneadenosine 
• 33485-36-8 N⁶-benzoyl-5'-O-benzoyladenosine 
• 674791-57-2 N-{9-[6-(1-hydroxy-pentyl)-2,2-dimethyl-tetrahydro-furo[3,4-d][1,3]dioxol-4-yl]-9H-purin-6-yl}-benzamide 
• 43077-04-9 6-N-benzoyl-9-(2,3-O-isopropylidene-β-D-ribo-pentodialdo-1,5-furanosyl)adeninehydrate 
• 68224-54-4 N-(9-((3aR,4R,6R,6aR)-6-((S)-1-hydroxyethyl)-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-yl)-9H-purin-6-yl)benzamide 
• 43077-03-8 N⁶-benzoyl-5'-deoxy-2',3'-O-isopropylidiene-5',5'-(N,N'-diphenylethylenediamino)adenosine 
• 43077-06-1 6-N-benzoyl-2',3'-O-isopropylideneadenosine-5'-aldehyde 

Relevant articles and documents

Stereoselective adenylate deaminase (5′-adenylic acid deaminase, AMPDA)-catalyzed deamination of 5′-alkyl substituted adenosines: A comparison with the action of adenosine deaminase (ADA)

The enzymes adenylate deaminase (AMPDA) and adenosine deaminase (ADA) are able to catalyze the stereoselective hydrolytic deamination of (5′R,S)-methyl-2′,3′-isopropylidene adenosine, but the 5′-butyl analog is a substrate only for AMPDA, which stereospec

Cyclonucleoside Formation and Ring Cleavage in the Reaction of 2',3'-O-Isopropylideneadenosine with Benzoyl Chloride and Its Substituted Derivatives

Reaction conditions suitable for the formation of 8,5'-O-cycloadenosine derivatives in the reaction of 2',3'-O-isopropylideneadenosine (1) with benzoyl chloride and substituted benzoyl chlorides were investigated.Thus, reaction of 1 with p-toluyl chloride