57620-56-1 Usage
Uses
Used in Chemical Synthesis:
2-(3-METHYL-3-NITROBUTYL)-1,3-DIOXOLANE is used as an intermediate in the synthesis of various chemical compounds, particularly those involving the dioxolane ring structure. Its unique functional groups allow for further chemical reactions and modifications, making it a versatile building block in organic chemistry.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2-(3-METHYL-3-NITROBUTYL)-1,3-DIOXOLANE is used as a precursor for the development of new drugs. Its chemical structure can be modified to create molecules with specific biological activities, potentially leading to the discovery of novel therapeutic agents.
Used in Material Science:
2-(3-METHYL-3-NITROBUTYL)-1,3-DIOXOLANE may also find applications in material science, where its unique structure could be utilized to create new materials with specific properties. These materials could have potential uses in various industries, such as electronics, automotive, or aerospace.
Used in Research and Development:
As a compound with a distinct chemical structure, 2-(3-METHYL-3-NITROBUTYL)-1,3-DIOXOLANE is used in research and development to study its properties and potential applications. This includes its use in the preparation of spin trap reagent, dimethyl-Δ′-pyrroline-1-oxide (DMPO), which is important for studying free radicals in chemical and biological systems.
Check Digit Verification of cas no
The CAS Registry Mumber 57620-56-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,6,2 and 0 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 57620-56:
(7*5)+(6*7)+(5*6)+(4*2)+(3*0)+(2*5)+(1*6)=131
131 % 10 = 1
So 57620-56-1 is a valid CAS Registry Number.
InChI:InChI=1/C8H15NO4/c1-8(2,9(10)11)4-3-7-12-5-6-13-7/h7H,3-6H2,1-2H3
57620-56-1Relevant academic research and scientific papers
Synthesis of 1-azaspiro[4.4]nonan-1-oxyls via intramolecular 1,3-dipolar cycloaddition
Khoroshunova, Yulia V.,Morozov, Denis A.,Taratayko, Andrey I.,Gladkikh, Polina D.,Glazachev, Yuri I.,Kirilyuk, Igor A.
, p. 2036 - 2042 (2019/09/30)
Sterically shielded nitroxides of the pyrrolidine series have shown the highest resistance to reduction. Here we report the synthesis of new pyrrolidine nitroxides from 5,5-dialkyl-1-pyrroline N-oxides via the introduction of a pent-4-enyl group to the nitrone carbon followed by an intramolecular 1,3-dipolar cycloaddition reaction and isoxazolidine ring opening. The kinetics of reduction of the new nitroxides with ascorbate were studied and compared to those of previously published (1S,2R,3′S,4′S,5′S,2″R)-dispiro[(2-hydroxymethyl)cyclopentan-1,2′-(3′,4′-di-tert-butoxy)pyrrolidine-5′,1″-(2″-hydroxymethyl)cyclopentane]-1′-oxyl (1).
Acylation of Aldo 1-Pyrroline 1-Oxides (4,5-Dihydro-3H-pyrrole 1-Oxides) and the Oxidation of the Resulting 3-Acyloxy-1-pyrrolines (3-Acyloxy-4,5-dihydro-3H-pyrroles)
Gibson, Neil J.,Forrester, Alexander R.
, p. 491 - 500 (2007/10/02)
5,5-Dimethyl-1-pyrroline 1-oxide (DMPO), when treated with NaH (1 mol) followed by ethyl chloroformate, benzoyl chloride, pivaloyl chloride or 2-bromoisobutyryl bromide gave the corresponding 3-acyloxy-1-pyrrolines.With NaH (2-4 mol) followed by benzoyl chloride or 2-bromoisobutyryl bromide, DMPO gave the corresponding 2-(3'-acyloxy-1'-pyrrolin-3'-yl)-3-acyloxypyrrolidines.Acylation of the 3-phenyl and 3-methyl DMPOs also gave the corresponding 3-acyloxy-1-pyrrolines.Oxidation of the 3-acyloxy-1-pyrrolines with m-CPBA gave the correspondong oxaziridines in good yield.These oxaziridines were resistant to ring opening by acid hydrolysis, photolysis and thermolysis.
