344790-86-9 Usage
Uses
Used in Electrochemical Applications:
1-Butyl-3-methylpyridinium bis(trifluormethylsulfonyl)imide is used as a modifier for electrodes in the detection of dopamine and uric acid in human urine samples. Its ability to enhance the sensitivity and selectivity of the detection process makes it a valuable component in the development of electrochemical sensors.
Used in Chemical Synthesis:
In the field of chemical synthesis, 1-Butyl-3-methylpyridinium bis(trifluormethylsulfonyl)imide serves as a solvent in the Ullmann homocoupling of aryl halides or aryl boronic acids using Cu nanoparticles. Its solvation properties facilitate the reaction, leading to improved yields and efficiency in the synthesis process.
Used in Medical Diagnostics:
1-Butyl-3-methylpyridinium bis(trifluormethylsulfonyl)imide is also used to modify the carbon paste electrode, which is applicable in the detection of dopamine in human serum and urine samples. Its incorporation into the electrode material enhances the performance of the sensor, allowing for more accurate and reliable measurements of dopamine levels in biological samples.
Check Digit Verification of cas no
The CAS Registry Mumber 344790-86-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,4,4,7,9 and 0 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 344790-86:
(8*3)+(7*4)+(6*4)+(5*7)+(4*9)+(3*0)+(2*8)+(1*6)=169
169 % 10 = 9
So 344790-86-9 is a valid CAS Registry Number.
InChI:InChI=1/C10H16N.C2F6NO4S2/c1-3-4-7-11-8-5-6-10(2)9-11;3-1(4,5)14(10,11)9-15(12,13)2(6,7)8/h5-6,8-9H,3-4,7H2,1-2H3;/q+1;-1
344790-86-9Relevant academic research and scientific papers
Nitrogen-containing ionic liquids: Biodegradation studies and utility in base-mediated reactions
Ford, Leigh,Ylijoki, Kai E.O.,Garcia, M. Teresa,Singer, Robert D.,Scammells, Peter J.
, p. 849 - 857 (2015/06/23)
Several ionic liquids (ILs) were prepared in order to study the susceptibility of various cores and substituents to biodegradability using the 'CO2 headspace' test (ISO 14593). Several of the ILs contained tertiary amine substituents and were tested as solvents and reagents for several base mediated processes including Suzuki-Miyaura, Sonogashira, Knoevenagel, and Morita-Baylis-Hilman reactions. It was found that although these ILs contain basic functionality, they do not promote base mediated reactions. Density functional theory molecular calculations confirmed that the protonation of these ILs is energetically unfavourable. Journal compilation
Ionic conducting gels, preparation method thereof and use of same
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Page/Page column 4, (2008/06/13)
A method of preparing an ionic conducting gel in solid form, known as ionogel. The method includes a step of mixing an ionic liquid with at least one molecular precursor containing at least one hydrolyzable group, if necessary in the presence of an acid, such as a carboxylic acid. The mixture is subsequently left to stand for one or more days until a gel is formed by polycondensation of the molecular precursor(s). The gel contains the aforementioned ionic liquid and can be set, in particular in transparent monolithic solid form.
