919530-72-6

Basic information

• Product Name: N-(9-{5-[bis-(4-methoxy-phenyl)-phenyl-methoxymethyl]-4-hydroxy-tetrahydro-furan-2-yl}-6-oxo-8-p-tolylamino-6,9-dihydro-1H-purin-2-yl)-isobutyramide
• Synonyms: N-(9-{5-[bis-(4-methoxy-phenyl)-phenyl-methoxymethyl]-4-hydroxy-tetrahydro-furan-2-yl}-6-oxo-8-p-tolylamino-6,9-dihydro-1H-purin-2-yl)-isobutyramide
• CAS NO: 919530-72-6
• Molecular Weight: 744.847
• Mol File: 919530-72-6.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: N-(9-{5-[bis-(4-methoxy-phenyl)-phenyl-methoxymethyl]-4-hydroxy-tetrahydro-furan-2-yl}-6-oxo-8-p-tolylamino-6,9-dihydro-1H-purin-2-yl)-isobutyramide(CAS DataBase Reference)
• NIST Chemistry Reference: N-(9-{5-[bis-(4-methoxy-phenyl)-phenyl-methoxymethyl]-4-hydroxy-tetrahydro-furan-2-yl}-6-oxo-8-p-tolylamino-6,9-dihydro-1H-purin-2-yl)-isobutyramide(919530-72-6)
• EPA Substance Registry System: N-(9-{5-[bis-(4-methoxy-phenyl)-phenyl-methoxymethyl]-4-hydroxy-tetrahydro-furan-2-yl}-6-oxo-8-p-tolylamino-6,9-dihydro-1H-purin-2-yl)-isobutyramide(919530-72-6)

Safety Data

• Hazardous Substances Data: 919530-72-6(Hazardous Substances Data)

Upstream product

• 40615-36-9 4,4'-dimethoxytrityl chloride 
• 919530-65-7 N-[6-hydroxy-9-(4-hydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl)-8-p-tolylamino-9H-purin-2-yl]-isobutyramide 
• 106-49-0 p-toluidine 
• 13389-03-2 8-bromo-2'-deoxyguanosine 
• 479408-21-4 3',5'-O,O'-bis(tert-butyldimethylsilyl)-8-bromo-2'-deoxyguanosine 
• 479408-22-5 O⁶-benzyl-8-bromo-3',5'-O-bis(tert-butyldimethylsilyl)-2'-deoxyguanosine 
• 444594-32-5 N²-iso-butyryl-O⁶-benzyl-8-bromo-3',5'-bis-O-(tert-butyldimethylsilyl)-2'-deoxyguanosine 
• 444594-35-8 N²-isobutyryl-O⁶-benzyl-8N-(4-methylphenylamino)-3',5'-bis(tert-butyldimethylsilyl)-2'-deoxy-guanosine 
• 919530-66-8 N²-isobutyryl-8N-(4-methylphenylamino)-3',5'-bis(tert-butyldimethylsilyl)-2'-deoxyguanosine 
• 919530-65-7 N²-isobutyryl-8N-(4-methylphenylamino)-2'-deoxyguanosine 

Relevant articles and documents

Synthesis and properties of oligonucleotides containing C8-deoxyguanosine arylamine adducts of borderline carcinogens

C8-Arylamine-dG adducts of borderline carcinogens and the bladder and breast carcinogen 4-aminobiphenyl were prepared using cross-coupling chemistry. These adducts were converted into the corresponding C8-arylamine-5′-O- DMTr-2′-deoxyguanosine phosphorami