Sign In to View Organizational & Contract Pricing.
Select a Size
About This Item
Linear Formula:
NH2COCONH2
CAS Number:
Molecular Weight:
88.07
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
207-442-5
Beilstein/REAXYS Number:
1743262
MDL number:
Assay:
98%
Form:
powder
InChI
1S/C2H4N2O2/c3-1(5)2(4)6/h(H2,3,5)(H2,4,6)
InChI key
YIKSCQDJHCMVMK-UHFFFAOYSA-N
SMILES string
NC(=O)C(N)=O
assay
98%
form
powder
mp
>300 °C (lit.)
Quality Level
Looking for similar products? Visit Product Comparison Guide
Related Categories
Application
Oxamide can be used:
- As a precursor for the synthesis of ligands such as bis(benzimidazole) and Schiff base ligands formed by condensation with furfural.
- Carbon nitride (g-C3N4) nanotubes by self-assembly polymerization with urea.
- As a bridging ligand for the synthesis of binuclear IrIII complex [Ir2(μ2-oxamidato-N,N′,O,O′)(ptpy)4], ptpy = 2-(p-tolyl)pyridinato.
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Li-Na Zhu et al.
Inorganic chemistry, 46(4), 1297-1304 (2007-01-25)
Four heteronuclear complexes Mn(CuL)2(SCN)2 (1), {[Mn(CuL)2(mu-dca)2].2H2O}n (2), Zn(CuL)2(SCN)2 (3), and [Fe(CuL)(N3)2]2 (4) incorporating macrocyclic oxamide ligands have been synthesized and structurally characterized. L is the dianion of diethyl 5,6,7,8,15,16-hexahydro-6,7-dioxodibenzo[1,4,8,11]-tetraazacyclotetradecine-13,18-dicarboxylate, and dca is the dicyanamide. The structure of 1 or 3
Yun Fei Long et al.
Analytica chimica acta, 624(1), 128-132 (2008-08-19)
Light scattering (LS) signals have been applied for analytical detections, but the selectivity is poor. In order to improve the selectivity, pre-separation or new machines are generally considered. Differing from these methods, we synthesized a highly selective oxamide ligand, N',N'-bis
Sergey P Gavrish et al.
Dalton transactions (Cambridge, England : 2003), (41)(41), 4708-4714 (2007-10-18)
A comparison of the molecular structure of related nickel(II) complexes of the open-chain and 13-membered macrocyclic oxamide-derived ligands NiL(1).4H2O and NiL(2).3H2O revealed that the formation of an additional 6-membered chelate ring in the complex results in rather small changes in
Synthesis and Molecular Structure of the New Green Emitting Complex [Ir2(?2-oxamidato-N, N?, O, O?)(2-(p-tolyl)pyridinato)4]
Graf M, et al.
Zeitschrift fur Anorganische und Allgemeine Chemie, 639(7), 1090-1094 (2013)
E Armelin et al.
The Journal of organic chemistry, 66(24), 8076-8085 (2001-11-28)
The conformational properties of the oxalamide group and crystal structure of several polyoxalamides have been investigated by computational methods. First, a detailed quantum mechanical study of the conformational preferences of N,N'-dimethyloxalamide is reported. Results, which were obtained at the MP2/6-31G(d)
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service