454715-81-2

Basic information

• Product Name: 5-O-[(1,1-dimethylethyl)diphenylsilyl]-4-C-vinyl-3-O-benzyl-1,2-O-isopropylidene-α-D-ribofuranose
• Synonyms: 5-O-[(1,1-dimethylethyl)diphenylsilyl]-4-C-vinyl-3-O-benzyl-1,2-O-isopropylidene-α-D-ribofuranose
• CAS NO: 454715-81-2
• Molecular Weight: 544.763
• Mol File: 454715-81-2.mol

Chemical Properties

• CAS DataBase Reference: 5-O-[(1,1-dimethylethyl)diphenylsilyl]-4-C-vinyl-3-O-benzyl-1,2-O-isopropylidene-α-D-ribofuranose(CAS DataBase Reference)
• NIST Chemistry Reference: 5-O-[(1,1-dimethylethyl)diphenylsilyl]-4-C-vinyl-3-O-benzyl-1,2-O-isopropylidene-α-D-ribofuranose(454715-81-2)
• EPA Substance Registry System: 5-O-[(1,1-dimethylethyl)diphenylsilyl]-4-C-vinyl-3-O-benzyl-1,2-O-isopropylidene-α-D-ribofuranose(454715-81-2)

Safety Data

• Hazardous Substances Data: 454715-81-2(Hazardous Substances Data)

Upstream product

• 212970-72-4 {3-[(2,2-dimethyl-1,1-diphenyl-1-silapropoxy)methyl]-(1S,3R,4S,5R)-7,7-dimethyl-2,6,8-trioxa-4-(phenylmethoxy)bicyclo[3.3.0]oct-3-yl}methan-1-ol 
• 1779-49-3 Methyltriphenylphosphonium bromide 
• 454715-80-1 5-O-(tert-butyldiphenylsilyl)-3-O-benzyl-4-C-formyl-1,2-O-isopropylidene-α-D-erythropentofuranose 

Downstream Products

• 860651-66-7 1,2-di-O-acetyl-3-O-benzyl-5-O-tert-butyldiphenylsilyl-4-C-vinyl-α,β-D-ribofuranose 
• 860651-74-7 2'-deoxy-5'-O-dimethoxytrityl-4'-C-ethyluridine 
• 860651-71-4 3'-O-benzyl-5'-O-tert-butyldiphenylsilyl-2'-deoxy-4'-C-vinyluridine 
• 860651-69-0 2'-O-acetyl-3'-O-benzyl-5'-O-tert-butyldiphenylsilyl-4'-C-vinyluridine 

Relevant articles and documents

Synthesis of 4′-C-aminoalkyl-2′-O-methyl modified RNA and their biological properties

In this paper, we describe the synthesis of 4′-C-aminoalkyl-2′-O-methylnucleosides and the properties of RNAs containing these analogs. Phosphoramidites of 4′-C-aminoethyl and 4′-C-aminopropyl-2′-O-methyluridines were prepared using glucose as starting ma

Synthesis and application of 4′-C-alkylated uridines as probes for uracil-DNA glycosylase

The development of new synthetic probes to study the mechanism of Uracil-DNA glycosylase is described. 4′-C-Alkylated 2′-deoxyuridines were synthesized and incorporated site-specifically into oligonucleotides. These compounds were subsequently employed in