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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
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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
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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
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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
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