N-(formylcarbamoyl)-2-oxopropanamide

Base Information

Chemical Name:N-(formylcarbamoyl)-2-oxopropanamide
CAS No.:27284-91-9
Molecular Formula:C5H6N2O4
Molecular Weight:158.114
Hs Code.:
DSSTox Substance ID:DTXSID30550689
Wikidata:Q82430116

Synonyms:N-(formylcarbamoyl)-2-oxopropanamide;27284-91-9;N-formyl-N'-pyruvylurea;N-formyl-N'-pyruvoylurea;DTXSID30550689

Suppliers and Price of N-(formylcarbamoyl)-2-oxopropanamide

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 0 raw suppliers

Chemical Property of N-(formylcarbamoyl)-2-oxopropanamide

Chemical Property:

PSA：99.32000
LogP:0.23820
XLogP3:-0.1
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:1
Exact Mass:158.03275668
Heavy Atom Count:11
Complexity:211

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC(=O)C(=O)NC(=O)NC=O

Technology Process of N-(formylcarbamoyl)-2-oxopropanamide

There total 4 articles about N-(formylcarbamoyl)-2-oxopropanamide 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:

: 65-71-4,28806-14-6,691841-57-3
thymin

: 4433-40-3
5-hydroxymethyl uracil

: 2417-22-3,697787-37-4
5-methylbarbituric acid

: 27284-91-9
N¹-formyl-N²-pyruvylurea

: 13514-92-6
6-Hydroxydihydrothymine

: 20433-38-9
5,6-dihydroxyuracil

: 696-04-8
5,6-dihydrothymine

Guidance literature:: With Saline; In water; Product distribution; Mechanism; Ambient temperature; Irradiation; promotion effect of addition of 2,2,6,6-tetramethylpiperidine-1-oxyls, influence of various saturation gases;
DOI:10.1246/cl.1983.1471