1-<2-O-methoxalyl-2-C-(2-phenethyl)-3,5-O--β-D-arabino-pentofuranosyl>uracil

Base Information

Chemical Name:1-<2-O-methoxalyl-2-C-(2-phenethyl)-3,5-O--β-D-arabino-pentofuranosyl>uracil
CAS No.:175232-28-7
Molecular Formula:C₃₂H₄₈N₂O₁₀Si₂
Molecular Weight:676.912
Hs Code.:

1-<2-O-methoxalyl-2-C-(2-phenethyl)-3,5-O-<tetraisopropyldisiloxane-1,3-diyl>-β-D-arabino-pentofuranosyl>uracil

Synonyms:1-<2-O-methoxalyl-2-C-(2-phenethyl)-3,5-O--β-D-arabino-pentofuranosyl>uracil

Suppliers and Price of 1-<2-O-methoxalyl-2-C-(2-phenethyl)-3,5-O--β-D-arabino-pentofuranosyl>uracil

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of 1-<2-O-methoxalyl-2-C-(2-phenethyl)-3,5-O--β-D-arabino-pentofuranosyl>uracil

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 1-<2-O-methoxalyl-2-C-(2-phenethyl)-3,5-O--β-D-arabino-pentofuranosyl>uracil

There total 2 articles about 1-<2-O-methoxalyl-2-C-(2-phenethyl)-3,5-O--β-D-arabino-pentofuranosyl>uracil which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 60.0%

: 175232-26-5
1-<2-O-methoxalyl-2-C-(2-phenylethynyl)-3,5-O--β-D-arabino-pentofuranosyl>uracil

: 175232-28-7
1-<2-O-methoxalyl-2-C-(2-phenethyl)-3,5-O--β-D-arabino-pentofuranosyl>uracil

: (2'S)-2'-deoxy-2'-C-(2-phenethyl)-3',5'-O--uridine

: (2'R)-2'-deoxy-2'-C-(2-phenethyl)-3',5'-O--uridine

Guidance literature:: With hydrogen; palladium on activated charcoal; In ethyl acetate; for 23h; Yields of byproduct given; Ambient temperature;
DOI:10.1080/07328319608002378

Reference yield:

: 114262-46-3
1-<2-C-(2-phenylethynyl)-3,5-O-(1,1,3,3-tetraisopropyldisiloxane-1,3-diyl)-β-D-arabinofuranosyl>uracil

: 175232-28-7
1-<2-O-methoxalyl-2-C-(2-phenethyl)-3,5-O--β-D-arabino-pentofuranosyl>uracil

Guidance literature:: Multi-step reaction with 2 steps

1: 100 percent / DMAP / CH₂Cl₂ / 4 h / 0 °C

2: 60 percent / H₂ / Pd/C / ethyl acetate / 23 h / Ambient temperature

With dmap; hydrogen; palladium on activated charcoal; In dichloromethane; ethyl acetate;
DOI:10.1080/07328319608002378

Reference yield:

: 175232-28-7
1-<2-O-methoxalyl-2-C-(2-phenethyl)-3,5-O--β-D-arabino-pentofuranosyl>uracil

: (2'S)-2'-deoxy-2'-C-(2-phenethyl)-3',5'-O--uridine

: (2'R)-2'-deoxy-2'-C-(2-phenethyl)-3',5'-O--uridine

Guidance literature:: With 2,2'-azobis(isobutyronitrile); tri-n-butyl-tin hydride; In toluene; at 75 ℃; for 4.5h; Yield given. Yields of byproduct given. Title compound not separated from byproducts;
DOI:10.1080/07328319608002378