866724-08-5

Basic information

• Product Name: 3’,5’-O-bis(tert-butydimethylsilyl)-N²-phenoxyacetyl-2’-deoxyguanosine
• Synonyms: 3’,5’-O-bis(tert-butydimethylsilyl)-N²-phenoxyacetyl-2’-deoxyguanosine
• CAS NO: 866724-08-5
• Molecular Weight: 629.904
• Mol File: 866724-08-5.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 3’,5’-O-bis(tert-butydimethylsilyl)-N²-phenoxyacetyl-2’-deoxyguanosine(CAS DataBase Reference)
• NIST Chemistry Reference: 3’,5’-O-bis(tert-butydimethylsilyl)-N²-phenoxyacetyl-2’-deoxyguanosine(866724-08-5)
• EPA Substance Registry System: 3’,5’-O-bis(tert-butydimethylsilyl)-N²-phenoxyacetyl-2’-deoxyguanosine(866724-08-5)

Safety Data

• Hazardous Substances Data: 866724-08-5(Hazardous Substances Data)

Upstream product

• 14316-61-1 phenoxyacetic anhydride 
• 51549-35-0 3',5'-bis-O-(tert-butyldimethylsilyl)-2'-deoxyguanosine 
• 110522-71-9 N²-phenoxyacetyl-2’-deoxyguanosine 
• 18162-48-6 tert-butyldimethylsilyl chloride 
• 947393-11-5 3',5'-O-bis(tert-butyldimethylsilyl)-2-N-carbamoyldeoxyguanosine 

Downstream Products

• 1204045-46-4 2-N-phenoxyacetyl-6-O-p-toluenesulphonyl-3',5'-di-O-t-butyldimethylsilyl-2'-deoxyguanosine 
• 578-76-7 7-methylguanine 
• 1323344-95-1 3’-O-(tert-butyldimethylsilyl)-N²-phenoxyacetyl-2’-deoxyguanosine 
• 138406-87-8 N-[9-{5-[bis-(4-methoxy-phenyl)-phenyl-methoxymethyl]-4-hydroxy-tetrahydro-furan-2-yl}-6-(2-cyano-ethylsulfanyl)-9H-purin-2-yl]-2-phenoxy-acetamide 
• 138406-86-7 N-[6-(2-cyano-ethylsulfanyl)-9-(4-hydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl)-9H-purin-2-yl]-2-phenoxy-acetamide 
• 906320-57-8 C₄₅H₆₉N₅O₈SSi₂ 

Relevant articles and documents

O6-Alkylguanine DNA Alkyltransferase Repair Activity Towards Intrastrand Cross-Linked DNA is Influenced by the Internucleotide Linkage

Oligonucleotides containing an alkylene intrastrand cross-link (IaCL) between the O6-atoms of two consecutive 2′-deoxyguanosines (dG) were prepared by solid-phase synthesis. UV thermal denaturation studies of duplexes containing butylene and he

Synthesis of oligodeoxynucleotides incorporating 2-N-carbamoylguanine and evaluation of the hybridization properties

Previously, we reported 2-N-carbamoylguanine (cmG) as a guanine analog. We further studied the synthetic protocol and hybridization properties of oligodeoxynucleotides (ODNs) incorporating cmG. These ODNs were synthesized using the phosphoramidite of cmG