415707-14-1

Basic information

• Product Name: N²-acetyl-5'-O-(4,4'-dimethoxytrityl)-3'-O-{[(triisopropylsilyl)oxy]methyl}guanosine
• Synonyms: N²-acetyl-5'-O-(4,4'-dimethoxytrityl)-3'-O-{[(triisopropylsilyl)oxy]methyl}guanosine
• CAS NO: 415707-14-1
• Molecular Weight: 814.023
• Mol File: 415707-14-1.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: N²-acetyl-5'-O-(4,4'-dimethoxytrityl)-3'-O-{[(triisopropylsilyl)oxy]methyl}guanosine(CAS DataBase Reference)
• NIST Chemistry Reference: N²-acetyl-5'-O-(4,4'-dimethoxytrityl)-3'-O-{[(triisopropylsilyl)oxy]methyl}guanosine(415707-14-1)
• EPA Substance Registry System: N²-acetyl-5'-O-(4,4'-dimethoxytrityl)-3'-O-{[(triisopropylsilyl)oxy]methyl}guanosine(415707-14-1)

Safety Data

• Hazardous Substances Data: 415707-14-1(Hazardous Substances Data)

Upstream product

• 231957-27-0 N²-acetyl-5'-O-(4,4'-dimethoxytrityl)guanosine 
• 217300-17-9 chloromethoxy-triisopropyl-silane 
• 253586-28-6 triisopropylsilyl (ethylthio)methyl ether 
• 118-00-3 G 
• 40615-36-9 4,4'-dimethoxytrityl chloride 
• 13154-24-0 triisopropylsilyl chloride 
• 129681-72-7 N²-acetylguanosine 
• 30747-23-0 Acetic acid (2R,3R,4R,5R)-4-acetoxy-5-acetoxymethyl-2-(2-acetylamino-6-oxo-1,6-dihydro-purin-9-yl)-tetrahydro-furan-3-yl ester 

Relevant articles and documents

Reliable chemical synthesis of oligoribonucleotides (RNA) with 2′-O-[(triisopropylsilyl)oxy]methyl(2′-O-tom)-protected phosphoramidites

A method for the introduction of the 2′-O-[(triisopropylsilyl)oxy]methyl (=tom) group into N-acetylated, 5′-O-dimethoxytritylated ribonucleosides is presented. The corresponding 2′-O-tom-protected phosphoramidite building blocks were obtained in pure form and were successfully employed for the routine synthesis of oligoribonucleotides on DNA synthesizers. Under DNA coupling conditions (2.5 min coupling time for a 1.5-μmol synthesis scale) and with 5-(benzylthio)-1H-tetrazole (BTT) as activator, 2′-O-tom-protected phosphoramidites exhibited average coupling yields >99.4%. The combination of N-acetyl and 2′-O-tom protecting groups allowed a reliable and complete two-step deprotection, first with MeNH2 in EtOH/H2O and then with Bu4NF in THF, without concomitant destruction of the product RNA sequences.