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Vidarabine phosphate

Base Information Edit
  • Chemical Name:Vidarabine phosphate
  • CAS No.:29984-33-6
  • Molecular Formula:C10H14N5O7P
  • Molecular Weight:347.224
  • Hs Code.:29400090
  • European Community (EC) Number:249-990-8
  • UNII:106XV160TZ
  • DSSTox Substance ID:DTXSID401009318
  • Nikkaji Number:J17.878K
  • Wikipedia:Vidarabine_phosphate
  • Wikidata:Q6607436
  • NCI Thesaurus Code:C90789
  • ChEMBL ID:CHEMBL1230732
  • Mol file:29984-33-6.mol
Vidarabine phosphate

Synonyms:9-(5-O-Phosphono-beta-D-arabinofuranosyl)-9H-purin-6-amine;Adenine Arabinoside Monophosphate;Ara AMP;Ara-AMP;Arabinofuranosyladenine Monophosphate;Monophosphate, Adenine Arabinoside;Monophosphate, Arabinofuranosyladenine;Monophosphate, Vidarabine;Phosphate, Vidarabine;Vidarabine Monophosphate;Vidarabine Phosphate

Suppliers and Price of Vidarabine phosphate
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • Crysdot
  • Vidarabinemonophosphate 97%
  • 5g
  • $ 200.00
  • Biosynth Carbosynth
  • 9-(b-D-Arabinofuranosyl)adenine 5'-monophosphate
  • 25 g
  • $ 475.00
  • Biosynth Carbosynth
  • 9-(b-D-Arabinofuranosyl)adenine 5'-monophosphate
  • 10 g
  • $ 220.00
  • Biosynth Carbosynth
  • 9-(b-D-Arabinofuranosyl)adenine 5'-monophosphate
  • 2 g
  • $ 60.00
  • Biosynth Carbosynth
  • 9-(b-D-Arabinofuranosyl)adenine 5'-monophosphate
  • 1 g
  • $ 40.00
  • Biosynth Carbosynth
  • 9-(b-D-Arabinofuranosyl)adenine 5'-monophosphate
  • 5 g
  • $ 115.00
  • American Custom Chemicals Corporation
  • ADENINE-9-BETA-D-ARABINOFURANOSIDE-5'-MONOPHOSPHATE 95.00%
  • 10MG
  • $ 622.19
  • Alfa Aesar
  • 9-beta-D-Arabinofuranosyladenine-5'-monophosphate, 99%
  • 5g
  • $ 63.70
  • Alfa Aesar
  • 9-beta-D-Arabinofuranosyladenine-5'-monophosphate, 99%
  • 1g
  • $ 22.10
  • AK Scientific
  • Vidarabinemonophosphate
  • 5g
  • $ 205.00
Total 97 raw suppliers
Chemical Property of Vidarabine phosphate Edit
Chemical Property:
  • Appearance/Colour:White crystalline powder. 
  • Vapor Pressure:6.7E-27mmHg at 25°C 
  • Melting Point:213 °C 
  • Boiling Point:798.5 °C at 760 mmHg 
  • PKA:1.86±0.10(Predicted) 
  • Flash Point:436.7 °C 
  • PSA:195.88000 
  • Density:2.32 g/cm3 
  • LogP:-1.28180 
  • Storage Temp.:Store at 0°C 
  • Water Solubility.:Soluble in water at 4mg/ml 
  • XLogP3:-3.5
  • Hydrogen Bond Donor Count:5
  • Hydrogen Bond Acceptor Count:11
  • Rotatable Bond Count:4
  • Exact Mass:347.06308480
  • Heavy Atom Count:23
  • Complexity:481
Purity/Quality:

99% *data from raw suppliers

Vidarabinemonophosphate 97% *data from reagent suppliers

Safty Information:
  • Pictogram(s): HarmfulXn, ToxicT, IrritantXi 
  • Hazard Codes:Xn,T,Xi 
  • Statements: 20/22-40-23/24/25-36/37/38 
  • Safety Statements: 37/39-24/25-45-36/37/39-22-36-26 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:C1=NC(=C2C(=N1)N(C=N2)C3C(C(C(O3)COP(=O)(O)O)O)O)N
  • Isomeric SMILES:C1=NC(=C2C(=N1)N(C=N2)[C@H]3[C@H]([C@@H]([C@H](O3)COP(=O)(O)O)O)O)N
  • Description Vidarabine monophosphate, chemical name: 9-(5-O-Phosphono-beta-D-arabinofuranosyl)adenine is an anti deoxyribonucleic acid virus drug. IVidarabine triphosphate directly inhibits DNA polymerase and also acts as a chain terminator in DNA replication. An adenosine monophosphate analog in which ribose is replaced by an arabinose moiety. It is the monophosphate ester of VIDARABINE with antiviral and possibly antineoplastic properties.
  • Uses Antiviral. Disrupts viral DNA synthesis. Competitive viral DNA polymerase inhibitor. Active against herpes simplex and varicella zoster viruses in vivo.
Technology Process of Vidarabine phosphate

There total 23 articles about Vidarabine phosphate 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:
With Palladium catalyst particles; In acetone; at 50 ℃; for 8h;
Guidance literature:
With Palladium catalyst particles; In 1,4-dioxane; at 50 ℃; for 8h;
Guidance literature:
With Palladium catalyst particles; In tetrahydrofuran; at 50 ℃; for 8h;
Refernces Edit
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