169687-75-6

Basic information

• Product Name: N⁴-benzoyl-1-[3,5-(1,1,3,3-tetraisopropyldisiloxane-1,3-diyl)-2-O-(2,3,5-tri-O-benzoyl-β-D-ribofuranosyl)-β-D-ribofuranosyl]cytosine
• Synonyms: N⁴-benzoyl-1-[3,5-(1,1,3,3-tetraisopropyldisiloxane-1,3-diyl)-2-O-(2,3,5-tri-O-benzoyl-β-D-ribofuranosyl)-β-D-ribofuranosyl]cytosine
• CAS NO: 169687-75-6
• Molecular Weight: 1034.28
• Mol File: 169687-75-6.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: N⁴-benzoyl-1-[3,5-(1,1,3,3-tetraisopropyldisiloxane-1,3-diyl)-2-O-(2,3,5-tri-O-benzoyl-β-D-ribofuranosyl)-β-D-ribofuranosyl]cytosine(CAS DataBase Reference)
• NIST Chemistry Reference: N⁴-benzoyl-1-[3,5-(1,1,3,3-tetraisopropyldisiloxane-1,3-diyl)-2-O-(2,3,5-tri-O-benzoyl-β-D-ribofuranosyl)-β-D-ribofuranosyl]cytosine(169687-75-6)
• EPA Substance Registry System: N⁴-benzoyl-1-[3,5-(1,1,3,3-tetraisopropyldisiloxane-1,3-diyl)-2-O-(2,3,5-tri-O-benzoyl-β-D-ribofuranosyl)-β-D-ribofuranosyl]cytosine(169687-75-6)

Safety Data

• Hazardous Substances Data: 169687-75-6(Hazardous Substances Data)

Upstream product

• 6974-32-9 1-O-acetyl-2,3,5-tri-O-benzoyl-β-D-ribofuranose 
• 69304-43-4 1-[3,5-O-(1,1,3,3-tetraisopropyldisiloxane-1,3-diyl)-β-D-ribofuranosyl]-N⁴-benzoylcytosine 

Downstream Products

• 183282-02-2 N⁴-benzoyl-1-[5-O-(4,4'-dimethoxytrityl)-2-O-(2,3,5-tri-O-benzoyl-β-D-ribofuranosyl)-β-D-ribofuranosyl]cytosine 
• 183281-88-1 N⁴-benzoyl-1-[2-O-(2,3,5-tri-O-benzoyl-β-D-ribofuranosyl)-β-D-ribofuranosyl]cytosine 
• 169687-78-9 C₃₅H₃₃N₃O₁₂ 

Relevant articles and documents

Synthesis and properties of some 2'-O-D-ribofuranosyl-nucleosides

A high yield preparation of 9-(2-O-β-D-ribofuranosyl-β-D- ribofuranosyl)-adenine and its pyrimidine analogues has been achieved and their physico-chemical properties were investigated.

An efficient synthesis and physico-chemical properties of 2′-O-D-ribofuranosylnucleosides, minor tRNA components

A high yield preparation of 9-(2-O-β-D-ribofuranosyl-β-D-ribofuranosyl)adenine, guanine- and the pyrimidine analogs (cytosine, thymine and uracil base moiety) has been achieved, and the conformational properties of the ring systems were investigated using NMR spectroscopy and X-ray.