All Photos(2)
About This Item
Linear Formula:
NH2COCONH2
CAS Number:
Molecular Weight:
88.07
Beilstein:
1743262
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
form:
powder
Assay:
98%
Pricing and availability is not currently available.
Recommended Products
Quality Level
Assay
98%
form
powder
mp
>300 °C (lit.)
SMILES string
NC(=O)C(N)=O
InChI
1S/C2H4N2O2/c3-1(5)2(4)6/h(H2,3,5)(H2,4,6)
InChI key
YIKSCQDJHCMVMK-UHFFFAOYSA-N
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)[1] and Schiff base ligands formed by condensation with furfural.[2][3]
- Carbon nitride (g-C3N4) nanotubes by self-assembly polymerization with urea.[4]
- 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.[5]
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
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.
Customers Also Viewed
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)
Synthesis, spectral, thermal and biological studies of mixed ligand complexes with newly prepared Schiff base and 1, 10-phenanthroline ligands
El-Halim HFA, et al.
Journal of Molecular Structure, 1146, 153-163 (2017)
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
S R Khan et al.
Scanning electron microscopy, (Pt 3)(Pt 3), 155-162 (1981-01-01)
The formation of urinary oxamide stones was induced in rats by feeding them oxamide mixed with powdered rat chow. The structure of these stones and the changes in the rat renal papillary structure following oxamide administration were studied using bright
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
Active Filters
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
