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5-Benzoyluridine

Base Information
  • Chemical Name:5-Benzoyluridine
  • CAS No.:85372-91-4
  • Molecular Formula:C16H16 N2 O7
  • Molecular Weight:348.312
  • Hs Code.:
  • European Community (EC) Number:286-748-0
  • DSSTox Substance ID:DTXSID60234546
  • Nikkaji Number:J310.323D
  • Wikidata:Q83116346
  • Mol file:85372-91-4.mol
5-Benzoyluridine

Synonyms:5-Benzoyluridine;85372-91-4;EINECS 286-748-0;SCHEMBL7101690;DTXSID60234546;ANFJQBUYDIHRPP-BPGGGUHBSA-N;NS00038887

Suppliers and Price of 5-Benzoyluridine
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 3 raw suppliers
Chemical Property of 5-Benzoyluridine
Chemical Property:
  • PSA:142.11000 
  • Density:1.577g/cm3 
  • LogP:-1.20860 
  • Storage Temp.:-20°C 
  • XLogP3:-0.4
  • Hydrogen Bond Donor Count:4
  • Hydrogen Bond Acceptor Count:7
  • Rotatable Bond Count:4
  • Exact Mass:348.09575085
  • Heavy Atom Count:25
  • Complexity:599
Purity/Quality:

98%Min *data from raw suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:C1=CC=C(C=C1)C(=O)C2=CN(C(=O)NC2=O)C3C(C(C(O3)CO)O)O
  • Isomeric SMILES:C1=CC=C(C=C1)C(=O)C2=CN(C(=O)NC2=O)[C@H]3[C@@H]([C@@H]([C@H](O3)CO)O)O
Technology Process of 5-Benzoyluridine

There total 11 articles about 5-Benzoyluridine 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 trifluoroacetic acid; for 72h; Ambient temperature;
DOI:10.1016/S0040-4020(01)96481-6
Guidance literature:
Multi-step reaction with 4 steps
1: hydrogen / 5percent Rh on alumina / methanol
2: 1.) LDA / 1.) THF, -70 deg C; 2.) THF, -70 deg C, 1 h
3: 1.) PhSeCl-pyridine; 2.) 30percent H2O2 / 1.) CH2Cl2, 0 deg C, rt overnight; 2.) CH2Cl2, 0 deg C, 2 h
4: 84.3 percent / 50percent aqueous trifluoroacetic acid
With pyridine; Phenylselenyl chloride; hydrogen; dihydrogen peroxide; trifluoroacetic acid; lithium diisopropyl amide; rhodium on alumina; In methanol;
DOI:10.1248/cpb.30.4589
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