5423-20-1 Usage
Uses
Used in Organic Synthesis:
1H-imidazole-4,5-di(carbohydrazide) is utilized as a reagent in organic synthesis for its ability to participate in a variety of chemical reactions, contributing to the formation of new compounds with potential applications in various fields.
Used in Pharmaceutical Research:
In pharmaceutical research, 1H-imidazole-4,5-di(carbohydrazide) serves as a key intermediate, facilitating the development of new drugs and therapeutic agents due to its unique chemical properties and reactivity.
Used as a Chelating Agent:
1H-imidazole-4,5-di(carbohydrazide) is employed as a chelating agent in various applications, capitalizing on its capability to form stable complexes with metal ions, which can be instrumental in processes such as metal recovery, purification, and the stabilization of metal-containing compounds.
Used in Polymer Production:
1H-imidazole-4,5-di(carbohydrazide) is used in the production of polymers, where its chemical structure contributes to the formation of polymeric materials with specific properties, such as enhanced stability or reactivity.
Used as a Corrosion Inhibitor for Metals:
1H-imidazole-4,5-di(carbohydrazide) functions as a corrosion inhibitor for metals, protecting them from degradation and extending their service life in various industrial applications.
Used in Analytical Chemistry:
As a reagent in analytical chemistry, 1H-imidazole-4,5-di(carbohydrazide) aids in the identification, measurement, and analysis of other substances, taking advantage of its reactivity and coordination capabilities.
Check Digit Verification of cas no
The CAS Registry Mumber 5423-20-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,2 and 3 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 5423-20:
(6*5)+(5*4)+(4*2)+(3*3)+(2*2)+(1*0)=71
71 % 10 = 1
So 5423-20-1 is a valid CAS Registry Number.
InChI:InChI=1/C5H8N6O2/c6-10-4(12)2-3(5(13)11-7)9-1-8-2/h1H,6-7H2,(H,8,9)(H,10,12)(H,11,13)
5423-20-1Relevant academic research and scientific papers
Triethylamine-templated nanocalix Ln12 clusters of diacylhydrazone: crystal structures and magnetic properties
Luo, Zhi-Rong,Zou, Hua-Hong,Chen, Zi-Lu,Li, Bo,Wang, Kai,Liang, Fu-Pei
supporting information, p. 17414 - 17421 (2019/12/02)
Three {Ln12} (Ln = Gd (1), Tb (2), Dy (3)) nanocalix clusters with a novel ligand of N,N′-bis(o-vanillidene)-1H-imidazole-4,5-dicarbohydrazide (H5ovih) were synthesized via the amine-templating strategy. The skeletal structures of these clusters were constructed from three symmetric {Ln4} units via the linkage of three V-type ligands, with a calix shape, which has not been reported previously. Complex 1 exhibited a clear magnetocaloric effect (MCE), whose maximum -ΔSm value reached 36.77 J kg-1 K-1 at 70 kOe and 2.0 K.
Syntheses and characterizations of imidazole-4,5-diacylhydrazones
Su, Guifa,Qin, Jiangke,Ni, Qingling,Mu, Hongtao
, p. 2429 - 2435 (2007/10/03)
Tartaric acid was transformed into imidazole-4,5-dicarboxylic acids 2, then via esterification, hydrazinolysis, condensation with aromatic aldehyde in glacial acetic acid to furnish seven title compounds in about 24% overall yield.
