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Merck
CN

O9328

Oxamide

98%

Synonym(s):

Oxalic acid diamide

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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
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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

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 [Ir22-oxamidato-N,N′,O,O′)(ptpy)4], ptpy = 2-(p-tolyl)pyridinato.



pictograms

Exclamation mark

signalword

Warning

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



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T L Nguyen et al.
Journal of the American Chemical Society, 123(44), 11057-11064 (2001-11-01)
Ureas characteristically form one-dimensional hydrogen-bonded alpha-networks with a repeat distance of about 4.60 A. Oxamides form similar alpha-networks with a longer 5.05 A repeat distance. The urea of glycine and the oxamide of glycine were each cocrystallized with a series
Advancing the n?π* electron transition of carbon nitride nanotubes for H2 photosynthesis
Zhang G, et al.
Journal of Material Chemistry A, 5(25), 12723-12728 (2017)
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)



Global Trade Item Number

SKUGTIN
O9328-100G04061838355324