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1-((2R,3S,4S,5R)-4-hydroxy-5-(hydroxymethyl)-3-methyltetrahydrofuran-2-yl)pyrimidine-2,4(1H,3H)-dione

Base Information
  • Chemical Name:1-((2R,3S,4S,5R)-4-hydroxy-5-(hydroxymethyl)-3-methyltetrahydrofuran-2-yl)pyrimidine-2,4(1H,3H)-dione
  • CAS No.:151384-15-5
  • Molecular Formula:C10H14N2O5
  • Molecular Weight:242.232
  • Hs Code.:
1-((2R,3S,4S,5R)-4-hydroxy-5-(hydroxymethyl)-3-methyltetrahydrofuran-2-yl)pyrimidine-2,4(1H,3H)-dione

Synonyms:1-((2R,3S,4S,5R)-4-hydroxy-5-(hydroxymethyl)-3-methyltetrahydrofuran-2-yl)pyrimidine-2,4(1H,3H)-dione

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Chemical Property of 1-((2R,3S,4S,5R)-4-hydroxy-5-(hydroxymethyl)-3-methyltetrahydrofuran-2-yl)pyrimidine-2,4(1H,3H)-dione
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Technology Process of 1-((2R,3S,4S,5R)-4-hydroxy-5-(hydroxymethyl)-3-methyltetrahydrofuran-2-yl)pyrimidine-2,4(1H,3H)-dione

There total 1 articles about 1-((2R,3S,4S,5R)-4-hydroxy-5-(hydroxymethyl)-3-methyltetrahydrofuran-2-yl)pyrimidine-2,4(1H,3H)-dione 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 5 steps
1: 100 percent / ammonia gas / methanol / 48 h / 0 - 4 °C
2: 65 percent / imidazole / dimethylformamide / 2 h / 20 °C
3: DMAP / acetonitrile / 1 h / 20 °C
4: 0.502 g / 2,2'-azobisisobutyronitrile; tributyltin hydride / toluene / 2 h / Heating
5: TBAF / tetrahydrofuran / 1 h / 20 °C
With 1H-imidazole; dmap; 2,2'-azobis(isobutyronitrile); tetrabutyl ammonium fluoride; ammonia; tri-n-butyl-tin hydride; In tetrahydrofuran; methanol; N,N-dimethyl-formamide; toluene; acetonitrile;
DOI:10.1021/jo034263y
Guidance literature:
Multi-step reaction with 5 steps
1: 1H-imidazole; iodine; triphenylphosphine / tetrahydrofuran
2: sodium methylate / methanol
3: benzyl triethylammonium azide; iodine; 4-methylmorpholine N-oxide / tetrahydrofuran
4: dmap / tetrahydrofuran; 1-methyl-pyrrolidin-2-one
5: ammonium bisulphate; 3-chloro-benzenecarboperoxoic acid / dichloromethane
With 1H-imidazole; dmap; ammonium bisulphate; benzyl triethylammonium azide; iodine; sodium methylate; 4-methylmorpholine N-oxide; 3-chloro-benzenecarboperoxoic acid; triphenylphosphine; In tetrahydrofuran; 1-methyl-pyrrolidin-2-one; methanol; dichloromethane;
DOI:10.1016/j.bmcl.2012.03.021
Guidance literature:
Multi-step reaction with 5 steps
1.1: 1H-imidazole; iodine; triphenylphosphine / tetrahydrofuran / 70.33 h / 0 - 20 °C
2.1: sodium methylate / methanol / 5 h / 60 °C
2.2: pyridinium form DOWEX H+ / 0.08 h / 0 - 20 °C
3.1: 4-methyl-morpholine; sodium azide; N-benzyl-N,N,N-triethylammonium chloride; iodine / tetrahydrofuran; acetonitrile / 6 h / 0 - 20 °C
3.3: 0 - 5 °C
4.1: dipotassium hydrogenphosphate; 3-chloro-benzenecarboperoxoic acid / tetra(n-butyl)ammonium hydrogensulfate / dichloromethane; water / 19.5 h / 20 °C
4.2: 0.5 h / 20 °C
5.1: pyridine
With 4-methyl-morpholine; pyridine; 1H-imidazole; dipotassium hydrogenphosphate; sodium azide; N-benzyl-N,N,N-triethylammonium chloride; iodine; sodium methylate; 3-chloro-benzenecarboperoxoic acid; triphenylphosphine; tetra(n-butyl)ammonium hydrogensulfate; In tetrahydrofuran; methanol; dichloromethane; water; acetonitrile;
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