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N3-benzoyl-1-(2'-O-benzoyl-β-D-ribopyranosyl)thymine

Base Information Edit
  • Chemical Name:N3-benzoyl-1-(2'-O-benzoyl-β-D-ribopyranosyl)thymine
  • CAS No.:245074-25-3
  • Molecular Formula:C24H22N2O8
  • Molecular Weight:466.447
  • Hs Code.:
  • Mol file:245074-25-3.mol
N<sup>3</sup>-benzoyl-1-(2'-O-benzoyl-β-D-ribopyranosyl)thymine

Synonyms:N3-benzoyl-1-(2'-O-benzoyl-β-D-ribopyranosyl)thymine

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Chemical Property of N3-benzoyl-1-(2'-O-benzoyl-β-D-ribopyranosyl)thymine Edit
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Technology Process of N3-benzoyl-1-(2'-O-benzoyl-β-D-ribopyranosyl)thymine

There total 4 articles about N3-benzoyl-1-(2'-O-benzoyl-β-D-ribopyranosyl)thymine 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:
Guidance literature:
1-(β-D-ribopyranosyl)thymine; With p-Anisaldehyde dimethyl acetal; toluene-4-sulfonic acid; In N,N-dimethyl-formamide; at 55 ℃; under 24.752 Torr;
benzoyl chloride; With dmap; In pyridine; at 20 ℃; for 16h;
With trifluoroacetic acid; In tetrahydrofuran; methanol; at 20 ℃; for 1h;
DOI:10.1002/hlca.200390349
Guidance literature:
Multi-step reaction with 3 steps
1.1: 90 percent / bis(trimethylsilyl)acetamide; TMS-OTf / acetonitrile / 3 h / 60 °C
2.1: 82 percent / NH3 / methanol / 18 h / 20 °C
3.1: TsOH*H2O; p-methoxybenzaldehyde dimethyl acetal / dimethylformamide / 55 °C / 24.75 Torr
3.2: DMAP / pyridine / 16 h / 20 °C
3.3: 8.1 g / CF3COOH / methanol; tetrahydrofuran / 1 h / 20 °C
With trimethylsilyl trifluoromethanesulfonate; p-Anisaldehyde dimethyl acetal; ammonia; toluene-4-sulfonic acid; bis-(trimethylsilyl)acetamide; In methanol; N,N-dimethyl-formamide; acetonitrile;
DOI:10.1002/hlca.200390349
Guidance literature:
Multi-step reaction with 3 steps
1.1: 90 percent / bis(trimethylsilyl)acetamide; TMS-OTf / acetonitrile / 3 h / 60 °C
2.1: 82 percent / NH3 / methanol / 18 h / 20 °C
3.1: TsOH*H2O; p-methoxybenzaldehyde dimethyl acetal / dimethylformamide / 55 °C / 24.75 Torr
3.2: DMAP / pyridine / 16 h / 20 °C
3.3: 8.1 g / CF3COOH / methanol; tetrahydrofuran / 1 h / 20 °C
With trimethylsilyl trifluoromethanesulfonate; p-Anisaldehyde dimethyl acetal; ammonia; toluene-4-sulfonic acid; bis-(trimethylsilyl)acetamide; In methanol; N,N-dimethyl-formamide; acetonitrile;
DOI:10.1002/hlca.200390349
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