105163-75-5 Usage
Uses
Used in Organic Synthesis:
Pyridinium, 4-[2-(benzoylthio)ethyl]-1-methyl-, iodide is used as a phase-transfer catalyst for facilitating various organic synthesis reactions. Its unique structure allows it to act as a bridge between the reactants in different phases, improving the efficiency and selectivity of the reactions.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, Pyridinium, 4-[2-(benzoylthio)ethyl]-1-methyl-, iodide is utilized as a catalyst in the synthesis of various active pharmaceutical ingredients. Its ability to enhance the reactivity and selectivity of reactions helps in the production of high-quality and cost-effective drugs.
Used in Chemical Research:
Pyridinium, 4-[2-(benzoylthio)ethyl]-1-methyl-, iodide is employed as a catalyst in various chemical research applications. Its strong catalytic properties and structural versatility make it a valuable tool for exploring new reaction pathways and developing innovative synthetic methods.
Used in Environmental Applications:
Pyridinium, 4-[2-(benzoylthio)ethyl]-1-methyl-, iodide can be used as a catalyst in environmental applications, such as the degradation of pollutants and the synthesis of environmentally friendly materials. Its ability to enhance reaction efficiency and selectivity can contribute to the development of sustainable chemical processes.
Check Digit Verification of cas no
The CAS Registry Mumber 105163-75-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,5,1,6 and 3 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 105163-75:
(8*1)+(7*0)+(6*5)+(5*1)+(4*6)+(3*3)+(2*7)+(1*5)=95
95 % 10 = 5
So 105163-75-5 is a valid CAS Registry Number.
105163-75-5Relevant academic research and scientific papers
2-(4-Pyridyl)ethyl as a Protective Group for Sulfur Functionality
Katritzky, Alan R.,Takahashi, Ichiro,Marson, Charles M.
, p. 4914 - 4920 (2007/10/02)
2-(4-Pyridyl)ethyl sulfides have been prepared from a variety of alkyl and aryl thiols and from alkyl and acyl halides.These sulfides and their corresponding sulfoxides and sulfones were each depyridylethylated by quaternization and subsequent treatment with mild base to give respectively the thiols, sulfenic acids, sulfinic acids, and sulfenamides.During one of these protection-deprotection sequences, methyl 1-octyl sulfoxide was readily converted by aerial oxidation into the corresponding sulfone.
