479408-29-2

Basic information

• Product Name: (3-{6-benzyloxy-2-{[bis-(4-methoxy-phenyl)-phenyl-methyl]-amino}-9-[4-(tert-butyl-dimethyl-silanyloxy)-5-(tert-butyl-dimethyl-silanyloxymethyl)-tetrahydro-furan-2-yl]-9H-purin-8-ylamino}-phenyl)-phenyl-methanone
• Synonyms: (3-{6-benzyloxy-2-{[bis-(4-methoxy-phenyl)-phenyl-methyl]-amino}-9-[4-(tert-butyl-dimethyl-silanyloxy)-5-(tert-butyl-dimethyl-silanyloxymethyl)-tetrahydro-furan-2-yl]-9H-purin-8-ylamino}-phenyl)-phenyl-methanone
• CAS NO: 479408-29-2
• Molecular Weight: 1083.49
• Mol File: 479408-29-2.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (3-{6-benzyloxy-2-{[bis-(4-methoxy-phenyl)-phenyl-methyl]-amino}-9-[4-(tert-butyl-dimethyl-silanyloxy)-5-(tert-butyl-dimethyl-silanyloxymethyl)-tetrahydro-furan-2-yl]-9H-purin-8-ylamino}-phenyl)-phenyl-methanone(CAS DataBase Reference)
• NIST Chemistry Reference: (3-{6-benzyloxy-2-{[bis-(4-methoxy-phenyl)-phenyl-methyl]-amino}-9-[4-(tert-butyl-dimethyl-silanyloxy)-5-(tert-butyl-dimethyl-silanyloxymethyl)-tetrahydro-furan-2-yl]-9H-purin-8-ylamino}-phenyl)-phenyl-methanone(479408-29-2)
• EPA Substance Registry System: (3-{6-benzyloxy-2-{[bis-(4-methoxy-phenyl)-phenyl-methyl]-amino}-9-[4-(tert-butyl-dimethyl-silanyloxy)-5-(tert-butyl-dimethyl-silanyloxymethyl)-tetrahydro-furan-2-yl]-9H-purin-8-ylamino}-phenyl)-phenyl-methanone(479408-29-2)

Safety Data

• Hazardous Substances Data: 479408-29-2(Hazardous Substances Data)

Upstream product

• 2835-78-1 3-amino benzophenone 
• 479408-23-6 O⁶-benzyl-8-bromo-3′,5′-O-bis(tert-butyldimethylsilyl)-N²-dimethoxytrityl-2′-deoxyguanosine 
• 479408-22-5 O⁶-benzyl-8-bromo-3',5'-O-bis(tert-butyldimethylsilyl)-2'-deoxyguanosine 
• 479408-21-4 3',5'-O,O'-bis(tert-butyldimethylsilyl)-8-bromo-2'-deoxyguanosine 
• 13389-03-2 8-bromo-2'-deoxyguanosine 
• 18162-48-6 tert-butyldimethylsilyl chloride 

Relevant articles and documents

Preparation of C8-amine and acetylamine adducts of 2′-deoxyguanosine suitably protected for DNA synthesis

(Equation presented) C8-Amine and acetylamine adducts of 2′-deoxyguanosine were synthesized. Our approach provides solutions for the coupling of aromatic amines to a protected 8-bromo-2′-deoxyguanosine derivative, for the selective acetylation of the coup