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3-Oxo-3-ureidopropanoic acid

Base Information Edit
  • Chemical Name:3-Oxo-3-ureidopropanoic acid
  • CAS No.:542-07-4
  • Molecular Formula:C4H6N2O4
  • Molecular Weight:146.103
  • Hs Code.:
  • DSSTox Substance ID:DTXSID601258771
  • Nikkaji Number:J657.734B
  • Wikidata:Q27104645
  • Metabolomics Workbench ID:52501
  • Mol file:542-07-4.mol
3-Oxo-3-ureidopropanoic acid

Synonyms:Malonuric acid;3-oxo-3-ureidopropanoic acid;542-07-4;3-(carbamoylamino)-3-oxopropanoic acid;Propanoic acid,3-[(aminocarbonyl)amino]-3- oxo-;CHEBI:49049;DTXSID601258771;AKOS006291968;3-[(Aminocarbonyl)amino]-3-oxopropanoic acid;Q27104645

Suppliers and Price of 3-Oxo-3-ureidopropanoic acid
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
  • TRC
  • MalonuricAcid
  • 5mg
  • $ 150.00
  • Medical Isotopes, Inc.
  • MalonuricAcid
  • 50 mg
  • $ 2200.00
Total 0 raw suppliers
Chemical Property of 3-Oxo-3-ureidopropanoic acid Edit
Chemical Property:
  • XLogP3:-1
  • Hydrogen Bond Donor Count:3
  • Hydrogen Bond Acceptor Count:4
  • Rotatable Bond Count:2
  • Exact Mass:146.03275668
  • Heavy Atom Count:10
  • Complexity:176
Purity/Quality:

MalonuricAcid *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Canonical SMILES:C(C(=O)NC(=O)N)C(=O)O
  • Uses Malonuric Acid is produced during degradation of sodium barbiturates.
Technology Process of 3-Oxo-3-ureidopropanoic acid

There total 1 articles about 3-Oxo-3-ureidopropanoic acid 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 sodium hydroxide; In water; at 70 ℃; Rate constant; Mechanism; var. conc. NaOH, other substituted derivatives of barbituric acid;
upstream raw materials:

BARBITURIC ACID

Refernces Edit
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