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4-Oxo-pentanoic acid 11-((2R,3S,4R,5R)-4-hydroxy-2-[(4-methoxy-phenyl)-diphenyl-methoxymethyl]-5-{6-[2-(4-nitro-phenyl)-ethoxycarbonylamino]-purin-9-yl}-tetrahydro-furan-3-yloxy)-undecyl ester

Base Information Edit
  • Chemical Name:4-Oxo-pentanoic acid 11-((2R,3S,4R,5R)-4-hydroxy-2-[(4-methoxy-phenyl)-diphenyl-methoxymethyl]-5-{6-[2-(4-nitro-phenyl)-ethoxycarbonylamino]-purin-9-yl}-tetrahydro-furan-3-yloxy)-undecyl ester
  • CAS No.:191853-58-4
  • Molecular Formula:C55H64N6O12
  • Molecular Weight:1001.15
  • Hs Code.:
  • Mol file:191853-58-4.mol
4-Oxo-pentanoic acid 11-((2R,3S,4R,5R)-4-hydroxy-2-[(4-methoxy-phenyl)-diphenyl-methoxymethyl]-5-{6-[2-(4-nitro-phenyl)-ethoxycarbonylamino]-purin-9-yl}-tetrahydro-furan-3-yloxy)-undecyl ester

Synonyms:4-Oxo-pentanoic acid 11-((2R,3S,4R,5R)-4-hydroxy-2-[(4-methoxy-phenyl)-diphenyl-methoxymethyl]-5-{6-[2-(4-nitro-phenyl)-ethoxycarbonylamino]-purin-9-yl}-tetrahydro-furan-3-yloxy)-undecyl ester

Suppliers and Price of 4-Oxo-pentanoic acid 11-((2R,3S,4R,5R)-4-hydroxy-2-[(4-methoxy-phenyl)-diphenyl-methoxymethyl]-5-{6-[2-(4-nitro-phenyl)-ethoxycarbonylamino]-purin-9-yl}-tetrahydro-furan-3-yloxy)-undecyl ester
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Chemical Property of 4-Oxo-pentanoic acid 11-((2R,3S,4R,5R)-4-hydroxy-2-[(4-methoxy-phenyl)-diphenyl-methoxymethyl]-5-{6-[2-(4-nitro-phenyl)-ethoxycarbonylamino]-purin-9-yl}-tetrahydro-furan-3-yloxy)-undecyl ester Edit
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Technology Process of 4-Oxo-pentanoic acid 11-((2R,3S,4R,5R)-4-hydroxy-2-[(4-methoxy-phenyl)-diphenyl-methoxymethyl]-5-{6-[2-(4-nitro-phenyl)-ethoxycarbonylamino]-purin-9-yl}-tetrahydro-furan-3-yloxy)-undecyl ester

There total 10 articles about 4-Oxo-pentanoic acid 11-((2R,3S,4R,5R)-4-hydroxy-2-[(4-methoxy-phenyl)-diphenyl-methoxymethyl]-5-{6-[2-(4-nitro-phenyl)-ethoxycarbonylamino]-purin-9-yl}-tetrahydro-furan-3-yloxy)-undecyl ester 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:
Multi-step reaction with 9 steps
1: 68 percent / 1H-imidazole / tetrahydrofuran
2: 88 percent / 1.) NaH; 2.) NaI / acetonitrile / 1.) room temp., 20 min.; 2.) room temp. overnight
3: 94 percent / Bu4NF*3H2O / tetrahydrofuran / Ambient temperature
4: 86 percent / EDC*HCl, DMAP / CH2Cl2 / 3 h / Ambient temperature
5: 86 percent / 80percent AcOH / H2O / 0.5 h / 100 °C
6: (NH24)SO4 / dioxane / 3 h / Heating
7: CH2Cl2
8: 80percent AcOH / H2O / 1 h
9: 74 percent / pyridine / 24 h / Ambient temperature
With pyridine; 1H-imidazole; dmap; (NH24)SO4; tetrabutyl ammonium fluoride; sodium hydride; acetic acid; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; sodium iodide; In tetrahydrofuran; 1,4-dioxane; dichloromethane; water; acetonitrile;
DOI:10.1002/hlca.19970800313
Guidance literature:
Multi-step reaction with 6 steps
1: 86 percent / EDC*HCl, DMAP / CH2Cl2 / 3 h / Ambient temperature
2: 86 percent / 80percent AcOH / H2O / 0.5 h / 100 °C
3: (NH24)SO4 / dioxane / 3 h / Heating
4: CH2Cl2
5: 80percent AcOH / H2O / 1 h
6: 74 percent / pyridine / 24 h / Ambient temperature
With pyridine; dmap; (NH24)SO4; acetic acid; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In 1,4-dioxane; dichloromethane; water;
DOI:10.1002/hlca.19970800313
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