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Technology Process of Dihydropyrimidine-2,4,5(3H)-trione

Dihydropyrimidine-2,4,5(3H)-trione

Base Information
  • Chemical Name:Dihydropyrimidine-2,4,5(3H)-trione
  • CAS No.:496-76-4
  • Molecular Formula:C4H4N2O3
  • Molecular Weight:128.087
  • Hs Code.:2933599550
  • European Community (EC) Number:207-829-9
  • NSC Number:95958
  • UNII:438WJI1S49
  • DSSTox Substance ID:DTXSID40964293
  • Nikkaji Number:J27.896C
  • Mol file:496-76-4.mol
Dihydropyrimidine-2,4,5(3H)-trione

Synonyms:5-hydroxyuracil

Suppliers and Price of Dihydropyrimidine-2,4,5(3H)-trione
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
  • TRC
  • Isobarbituric acid
  • 500mg
  • $ 275.00
  • TRC
  • Isobarbituric acid
  • 250mg
  • $ 145.00
  • Sigma-Aldrich
  • Fluorouracil Related Compound B United States Pharmacopeia (USP) Reference Standard
  • 25mg
  • $ 1160.00
  • Sigma-Aldrich
  • Isobarbituric acid analytical standard
  • 1g
  • $ 117.00
  • Matrix Scientific
  • Isobarbituric acid 95%
  • 1g
  • $ 350.00
  • Matrix Scientific
  • Isobarbituric acid 95%
  • 5g
  • $ 1749.00
  • American Custom Chemicals Corporation
  • 5-HYDROXY-2,4(1H,3H)-PYRIMIDINEDIONE 95.00%
  • 5MG
  • $ 495.26
  • AK Scientific
  • Dihydropyrimidine-2,4,5(3H)-trione
  • 5g
  • $ 323.00
Total 33 raw suppliers
Chemical Property of Dihydropyrimidine-2,4,5(3H)-trione
Chemical Property:
  • Melting Point:>300 °C (dec.)(lit.)  
  • Refractive Index:1.492 
  • Boiling Point:534.5oC at 760mmHg 
  • PKA:8.25±0.20(Predicted) 
  • Flash Point:277oC 
  • PSA：85.95000 
  • Density:1.455g/cm3 
  • LogP:-1.23120 
  • Solubility.:Soluble in DMSO (Sparingly), Methanol (Sparingly). 
  • XLogP3:-1.2
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:3
  • Rotatable Bond Count:0
  • Exact Mass:128.02219199
  • Heavy Atom Count:9
  • Complexity:186
Purity/Quality:

97% *data from raw suppliers

Isobarbituric acid *data from reagent suppliers

Safty Information:
  • Pictogram(s): R36/37/38:Irritating to eyes, respiratory system and skin.; 
  • Hazard Codes:Xi 
  • Statements: 36/37/38 
  • Safety Statements: 26-36 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:C1C(=O)C(=O)NC(=O)N1
  • Uses A 5-hydroxy derivative of the nucleobase Uracil (U801000) and an isomer of Barbituric Acid (B118650). Studies show that it can form stable base pairs with all four bases in a DNA duplex. It has been u sed as oxidative DNA damage biomarker in tissue engineered skin 2,4,5-Trihydroxypyrimidine studies show that it can form stable base pairs with all four bases in a DNA duplex. It has been used as oxidative DNA damage biomarker in tissue engineered skin. It acts as an antagonist of uracil in the growth of Lactobacillus casei.
Technology Process of Dihydropyrimidine-2,4,5(3H)-trione

There total 1 articles about Dihydropyrimidine-2,4,5(3H)-trione 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:

Reference yield:

dihydropyrimidine-2,4,5(3H)-trione
496-76-4

dihydropyrimidine-2,4,5(3H)-trione

Guidance literature:
Uracil, H2O2, FeSO4, Ethylendiamin-tetraacetat-Na-salz, 37grad, in Phosphatlsg. bei pH 7.2;
Refernces

Isovioluric Acid (Alloxan-6-Oxime)

10.1073/pnas.18.7.490

The research investigates the chemical properties and transformations of isovioluric acid and its derivatives. The purpose of the study is to explore the behavior of isovioluric acid, an unusual oxime of alloxan, and its reduction products. Key chemicals involved include isovioluric acid (VI), which is derived from isobarbituric acid through the action of nitrous acid. This compound exhibits unique properties such as oxidation of potassium iodide and formation of colored salts. The study also examines the reduction of isovioluric acid to isouramil (XI) using ammonium sulfide, which resembles dialuric acid in its chemical properties and can be converted into dialuric acid (XII) by hydrochloric acid. The research concludes that isovioluric acid and its derivatives display distinct behaviors compared to related compounds like alloxan and violuric acid, providing new insights into the chemistry of these uracil derivatives and their potential applications in the study of purine group compounds.

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