786666-09-9

Basic information

• Product Name: (2S,3R,4R,5R)-3-Amino-4-(tert-butyl-dimethyl-silanyloxy)-5-[2-chloro-6-(3-iodo-benzylamino)-purin-9-yl]-tetrahydro-furan-2-carboxylic acid methylamide
• CAS NO: 786666-09-9
• Molecular Weight: 658.014
• Mol File: 786666-09-9.mol

Chemical Properties

• CAS DataBase Reference: (2S,3R,4R,5R)-3-Amino-4-(tert-butyl-dimethyl-silanyloxy)-5-[2-chloro-6-(3-iodo-benzylamino)-purin-9-yl]-tetrahydro-furan-2-carboxylic acid methylamide(CAS DataBase Reference)
• NIST Chemistry Reference: (2S,3R,4R,5R)-3-Amino-4-(tert-butyl-dimethyl-silanyloxy)-5-[2-chloro-6-(3-iodo-benzylamino)-purin-9-yl]-tetrahydro-furan-2-carboxylic acid methylamide(786666-09-9)
• EPA Substance Registry System: (2S,3R,4R,5R)-3-Amino-4-(tert-butyl-dimethyl-silanyloxy)-5-[2-chloro-6-(3-iodo-benzylamino)-purin-9-yl]-tetrahydro-furan-2-carboxylic acid methylamide(786666-09-9)

Safety Data

• Hazardous Substances Data: 786666-09-9(Hazardous Substances Data)

Upstream product

• 786666-01-1 (2S,3S,4R,5R)-3-Azido-5-[2-chloro-6-(3-iodo-benzylamino)-purin-9-yl]-4-hydroxy-tetrahydro-furan-2-carboxylic acid methylamide 
• 786665-97-2 9-[2-O-acetyl-3-C-azido-3-deoxy-5-(methylcarbamoyl)-β-D-ribofuranosyl]-2,6-dichloropurine 
• 331729-04-5 3-azido-3-deoxy-1,2-diacetoxy-α-D-ribofuranuronic acid methyl amide 
• 331729-05-6 3-azido-3-deoxy-1,2-O-isopropylidene-α-D-ribofuranuronic acid methyl amide 
• 582-52-5 1,2:5,6-di-O-isopropylidene-α-D-glucofuranose 
• 55951-93-4 1,2:5,6-di-O-isopropylidene-3-O-triflyl-α-D-glucofuranose 
• 21870-78-0 3-azido-3-deoxy-1,2:5,6-di-O-isopropylidene-α-D-allofuranose 
• 35085-25-7 3-azido-3-deoxy-1,2-O-isopropylidene-α-D-allofuranose 

Downstream Products

• 786666-17-9 (2S,3R,4R,5R)-4-(tert-Butyl-dimethyl-silanyloxy)-5-[2-chloro-6-(3-iodo-benzylamino)-purin-9-yl]-3-ureido-tetrahydro-furan-2-carboxylic acid methylamide 

Relevant articles and documents

Design and synthesis of 3′-ureidoadenosine-5′-uronamides: Effects of the 3′-ureido group on binding to the A3 adenosine receptor

Novel 3′-ureidoadenosine analogues, 3 and 4 were synthesized from 1,2:5,6-di-O-isopropylidene-d-glucose in order to cause stronger hydrogen bonding than the corresponding 3′-aminoadenosine derivatives at the A 3 adenosine receptor. On the basis