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Aracytidine 5'-O-phenylphosphate

Base Information
  • Chemical Name:Aracytidine 5'-O-phenylphosphate
  • CAS No.:17489-61-1
  • Molecular Formula:C15H18N3O8P
  • Molecular Weight:399.297
  • Hs Code.:
  • NSC Number:128280
  • DSSTox Substance ID:DTXSID40938595
  • ChEMBL ID:CHEMBL1969245
Aracytidine 5'-O-phenylphosphate

Synonyms:17489-61-1;Aracytidine 5'-O-phenylphosphate;CHEMBL1969245;DTXSID40938595;NSC128280;NSC-128280;2(1H)-Pyrimidinone, 4-amino-1-[5-O-(hydroxyphenoxyphosphinyl)-.beta.-D-arabinofuranosyl]-;Cytosinearabinoside 5'-O-phenylphosphate;Cytosine, 5'-(phenyl hydrogen phosphate);NCI60_000643;1-{5-O-[Hydroxy(phenoxy)phosphoryl]pentofuranosyl}-4-imino-1,4-dihydropyrimidin-2-ol

Suppliers and Price of Aracytidine 5'-O-phenylphosphate
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
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Total 1 raw suppliers
Chemical Property of Aracytidine 5'-O-phenylphosphate
Chemical Property:
  • Vapor Pressure:2.71E-18mmHg at 25°C 
  • Boiling Point:659.5°C at 760 mmHg 
  • Flash Point:352.7°C 
  • Density:1.75g/cm3 
  • XLogP3:-1.1
  • Hydrogen Bond Donor Count:4
  • Hydrogen Bond Acceptor Count:8
  • Rotatable Bond Count:6
  • Exact Mass:399.08315154
  • Heavy Atom Count:27
  • Complexity:665
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:C1=CC=C(C=C1)OP(=O)(O)OCC2C(C(C(O2)N3C=CC(=NC3=O)N)O)O
Technology Process of Aracytidine 5'-O-phenylphosphate

There total 5 articles about Aracytidine 5'-O-phenylphosphate 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 4 steps
1: 5 g / nuclease-3'-nucleotidase P1, CH3COONa, / H2O / 24 h / 60 °C
2: 1.) tri-n-butylamine 2.) H2) / 1.) pyridine, RT, 20 h, 2.) RT, 20 h,
3: 1.) TPS-Cl, / 1.) CHCl3, 2.) pyridine, RT, 5 h,
4: NH3 / ethanol
With tributyl-amine; Triphenylsilyl chloride; nuclease-3'-nucleotidase P1; ammonia; hydrogen; sodium acetate; In ethanol; water;
DOI:10.1248/cpb.28.2915
Guidance literature:
Multi-step reaction with 2 steps
1: 1.) TPS-Cl, / 1.) CHCl3, 2.) pyridine, RT, 5 h,
2: NH3 / ethanol
With Triphenylsilyl chloride; ammonia; In ethanol;
DOI:10.1248/cpb.28.2915
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