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2'-Deoxyuridine 5'-monophosphate

Base Information
  • Chemical Name:2'-Deoxyuridine 5'-monophosphate
  • CAS No.:964-26-1
  • Deprecated CAS:135556-16-0,87578-10-7
  • Molecular Formula:C9H13 N2 O8 P
  • Molecular Weight:308.185
  • Hs Code.:
  • European Community (EC) Number:213-518-9
  • UNII:N9J10KFG94
  • DSSTox Substance ID:DTXSID20242223
  • Nikkaji Number:J298.569A
  • Wikipedia:Deoxyuridine_monophosphate
  • Wikidata:Q2741362
  • Metabolomics Workbench ID:37779
  • ChEMBL ID:CHEMBL211312
2'-Deoxyuridine 5'-monophosphate

Synonyms:2'-deoxy-5'-uridylic acid;2'-deoxyuridine 5'-phosphate;2'-deoxyuridine-5'-monophosphate;2'-deoxyuridylic acid;2'-deoxyuridylic acid, disodium salt;dUMP

Suppliers and Price of 2'-Deoxyuridine 5'-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
  • Packaging
  • price
Total 9 raw suppliers
Chemical Property of 2'-Deoxyuridine 5'-monophosphate
Chemical Property:
  • Appearance/Colour:white powder 
  • XLogP3:-3.3
  • Hydrogen Bond Donor Count:4
  • Hydrogen Bond Acceptor Count:8
  • Rotatable Bond Count:4
  • Exact Mass:308.04095237
  • Heavy Atom Count:20
  • Complexity:488
Purity/Quality:

98%Min *data from raw suppliers

Safty Information:
  • Pictogram(s): UN NO. 
  • Hazard Codes:UN NO. 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:C1C(C(OC1N2C=CC(=O)NC2=O)COP(=O)(O)O)O
  • Isomeric SMILES:C1[C@@H]([C@H](O[C@H]1N2C=CC(=O)NC2=O)COP(=O)(O)O)O
Technology Process of 2'-Deoxyuridine 5'-monophosphate

There total 7 articles about 2'-Deoxyuridine 5'-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:
2'-deoxyuridine; With N,N,N',N'-tetramethyl-1,8-diaminonaphthalene; trichlorophosphate; at 20 ℃; for 0.25h; Flow reactor; Green chemistry;
With water; at 20 ℃; Temperature; chemoselective reaction; Flow reactor; Green chemistry;
DOI:10.1021/op5002066
Guidance literature:
With acetate buffer; bovine spleen phosphodiesterase II; at 37 ℃; for 1h; pH=6.0; Enzyme kinetics;
DOI:10.1016/j.bmcl.2003.07.034
Guidance literature:
With acetic acid; In water; at 50 ℃; for 5h;
DOI:10.1055/s-1982-29689
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