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Technology Process of ethyl [[(2R,3S,5R)-5-(2,4-dioxopyrimidin-1-yl)-3-hydroxy-tetrahydrofuran-2-yl]methoxy-methoxy-phosphoryl]formate

ethyl [[(2R,3S,5R)-5-(2,4-dioxopyrimidin-1-yl)-3-hydroxy-tetrahydrofuran-2-yl]methoxy-methoxy-phosphoryl]formate

Base Information
  • Chemical Name:ethyl [[(2R,3S,5R)-5-(2,4-dioxopyrimidin-1-yl)-3-hydroxy-tetrahydrofuran-2-yl]methoxy-methoxy-phosphoryl]formate
  • CAS No.:115365-13-4
  • Molecular Formula:C13H19 N2 O9 P
  • Molecular Weight:378.2717
  • Hs Code.:
  • ChEMBL ID:CHEMBL3144454
  • DSSTox Substance ID:DTXSID90921679
  • Mol file:115365-13-4.mol
ethyl [[(2R,3S,5R)-5-(2,4-dioxopyrimidin-1-yl)-3-hydroxy-tetrahydrofuran-2-yl]methoxy-methoxy-phosphoryl]formate

Synonyms:115365-13-4;CHEMBL3144454;DTXSID90921679;ethyl [[(2R,3S,5R)-5-(2,4-dioxopyrimidin-1-yl)-3-hydroxy-tetrahydrofuran-2-yl]methoxy-methoxy-phosphoryl]formate;[[1-(2,4-Dioxo-1,2,3,4-tetrahyropyrimidin-1-yl)-2-deoxy-Beta-D-erythro-pentofuranos-5-yl]oxy]methoxyphosphine-carboxylic acid ethyl ester oxide;1-{2-Deoxy-5-O-[(ethoxycarbonyl)(methoxy)phosphoryl]pentofuranosyl}-4-hydroxypyrimidin-2(1H)-one

Suppliers and Price of ethyl [[(2R,3S,5R)-5-(2,4-dioxopyrimidin-1-yl)-3-hydroxy-tetrahydrofuran-2-yl]methoxy-methoxy-phosphoryl]formate
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
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Total 5 raw suppliers
Chemical Property of ethyl [[(2R,3S,5R)-5-(2,4-dioxopyrimidin-1-yl)-3-hydroxy-tetrahydrofuran-2-yl]methoxy-methoxy-phosphoryl]formate
Chemical Property:
  • Boiling Point:°Cat760mmHg 
  • Flash Point:°C 
  • Density:1.467g/cm3 
  • XLogP3:-1.7
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:9
  • Rotatable Bond Count:8
  • Exact Mass:378.08281719
  • Heavy Atom Count:25
  • Complexity:623
Purity/Quality:

99% *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CCOC(=O)P(=O)(OC)OCC1C(CC(O1)N2C=CC(=O)NC2=O)O
  • Isomeric SMILES:CCOC(=O)P(=O)(OC)OC[C@@H]1[C@H](C[C@@H](O1)N2C=CC(=O)NC2=O)O
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