Select a Size
100 G
₹3,420.70
All Photos(2)
Select a Size
Change View
100 G
₹3,420.70
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%
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
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)
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
Bis (benzimidazole) as supramolecular building block in manganese (IV) chemistry
Samol'ova E, et al.
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
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
