32833-96-8 Usage
Uses
Used in Coordination Chemistry:
N,N-Dimethyloxamic acid is used as a chelating agent for forming stable coordination complexes with metal ions. This property is crucial in the field of coordination chemistry, where it aids in the study and manipulation of metal complexes.
Used in Analytical Chemistry:
In Analytical Chemistry, N,N-Dimethyloxamic acid is used as a reagent for detecting the presence of nickel, copper, and cobalt ions. Its ability to form stable complexes with these metal ions allows for their isolation and identification in various samples.
Used in Organic Synthesis:
N,N-Dimethyloxamic acid is employed in the preparation of other organic compounds, contributing to the synthesis of a range of chemical products. Its role as a catalyst in organic synthesis enhances the efficiency and selectivity of chemical reactions.
Used in Pharmaceutical and Agricultural Industries:
Although still under exploration, N,N-Dimethyloxamic acid has potential applications in the development of pharmaceuticals and agricultural products. Its unique properties may contribute to the creation of new drugs or agrochemicals, pending further research and development.
Safety Precautions:
It is important to handle N,N-Dimethyloxamic acid with care due to its corrosive nature. Appropriate safety measures should be taken to prevent skin and eye irritation, ensuring the well-being of those working with N,N-DIMETHYLOXAMICACID.
Check Digit Verification of cas no
The CAS Registry Mumber 32833-96-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,2,8,3 and 3 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 32833-96:
(7*3)+(6*2)+(5*8)+(4*3)+(3*3)+(2*9)+(1*6)=118
118 % 10 = 8
So 32833-96-8 is a valid CAS Registry Number.
InChI:InChI=1/C4H7NO3/c1-5(2)3(6)4(7)8/h1-2H3,(H,7,8)
32833-96-8Relevant articles and documents
A FACILE, CONVENIENT AND SELECTIVE HOMOLYTIC CARBAMOYLATION OF HETEROAROMATIC BASES
Coppa, Fausta,Fontana, Francesca,Lazzarini, Edoardo,Minisci, Francesco
, p. 2687 - 2696 (2007/10/02)
The oxidative decarboxylation of monoamides of oxalic acid provides carbamoyl radicals, which are useful for the selective carbamoylation of protonated heteroaromatic bases; this reaction represents the first general and selective method for the N-alkyl or N-arylcarbamoylation of heteroaromatic bases.Compared to alkoxycarbonylation, this reaction is much more effective and selective, owing to more favourable polar and enthalpic effects.The importance of the steric effects is also emphasized.
