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bis(3'-5')cyclic diuridine monophosphate

Base Information
  • Chemical Name:bis(3'-5')cyclic diuridine monophosphate
  • CAS No.:73120-97-5
  • Molecular Formula:C18H22N4O16P2
  • Molecular Weight:612.337
  • Hs Code.:
  • Mol file:73120-97-5.mol
bis(3'-5')cyclic diuridine monophosphate

Synonyms:Uridine,5'-O-phosphoryluridylyl-(3'® 5')-, cyclic nucleotide (7CI); 2H,7H-Difuro[3,2-d:3',2'-j][1,3,7,9,2,8]tetraoxadiphosphacyclododecin,3'-uridylic acid deriv.

Suppliers and Price of bis(3'-5')cyclic diuridine monophosphate
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 3 raw suppliers
Chemical Property of bis(3'-5')cyclic diuridine monophosphate
Chemical Property:
  • PSA:300.30000 
  • LogP:-2.55400 
Purity/Quality:

95% *data from raw suppliers

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

SDS file from LookChem

Useful:
Technology Process of bis(3'-5')cyclic diuridine monophosphate

There total 5 articles about bis(3'-5')cyclic diuridine monophosphate 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:
cy-r(2'-O-TOM)G(2'-O-TOM)U*2TEA; With tetrabutyl ammonium fluoride; In tetrahydrofuran; at 20 ℃; for 12h;
With Sephadex G 10; In water;
DOI:10.1002/(SICI)1521-3765(19990702)5:7<2077::AID-CHEM2077>3.0.CO;2-U
Guidance literature:
Multi-step reaction with 2 steps
1.1: MeNH2; H2O / ethanol / 20 °C
2.1: TBAF*3H2O / tetrahydrofuran / 12 h / 20 °C
2.2: Sephadex G 10 / H2O
With tetrabutyl ammonium fluoride; water; methylamine; In tetrahydrofuran; ethanol; 1.1: Deacetylation / 2.1: deetherification / 2.2: desalting;
DOI:10.1002/(SICI)1521-3765(19990702)5:7<2077::AID-CHEM2077>3.0.CO;2-U
Guidance literature:
With triethylamine tris(hydrogen fluoride); at 20 ℃; for 12h;
DOI:10.1016/j.bmc.2010.07.068
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