4360-58-1 Usage
Uses
Used in Solvent Applications:
2,4,4,5,5-Pentamethyl-1,3-dioxolane is used as a solvent for its ability to dissolve a wide range of organic compounds. Its stability and non-reactivity make it a preferred choice in various industrial processes.
Used in Chemical Synthesis:
In the Chemical Synthesis Industry, 2,4,4,5,5-pentamethyl-1,3-dioxolane is used as a reagent or intermediate in the production of various chemical compounds due to its solubility properties and compatibility with a broad spectrum of organic materials.
Used in Industrial Processes:
2,4,4,5,5-Pentamethyl-1,3-dioxolane is utilized in various industrial processes as a process solvent, taking advantage of its low toxicity and general safety profile when used with proper safety measures.
Used in Research and Development:
In the Research and Development sector, 2,4,4,5,5-pentamethyl-1,3-dioxolane serves as a valuable compound for testing and experimentation, given its unique properties and wide applicability in chemical reactions and processes.
Check Digit Verification of cas no
The CAS Registry Mumber 4360-58-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,3,6 and 0 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 4360-58:
(6*4)+(5*3)+(4*6)+(3*0)+(2*5)+(1*8)=81
81 % 10 = 1
So 4360-58-1 is a valid CAS Registry Number.
4360-58-1Relevant academic research and scientific papers
Catalytic migratory oxidative coupling of nitrones
Hashizume, Shogo,Oisaki, Kounosuke,Kanai, Motomu
supporting information; experimental part, p. 4288 - 4291 (2011/10/09)
A Cu(I)-catalyzed migratory oxidative coupling between nitrones and heterocycles or a methylamine is described. Selective C-C bond-formation proceeds through cleavage of two C(sp3)-H bonds concomitant with C=N double bond-migration. The reaction provides an alternating nitrone moiety, allowing for further synthetically useful transformations. Radical clock studies suggest that the nucleophilic addition of nitrones to an oxidatively generated carbocation is a key step.
