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100 G
$81.10
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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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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Bis (benzimidazole) as supramolecular building block in manganese (IV) chemistry
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Journal of Molecular Structure, 1176, 366-375 (2019)
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)
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
Synthesis, characterization, and biological and anticancer studies of mixed ligand complexes with Schiff base and 2, 2?-bipyridine
Omar MM, et al.
Applied Organometallic Chemistry, 31(10), e3724-e3724 (2017)
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
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