54288-69-6 Usage
Uses
Used in Ionic Liquids Synthesis:
2-(chloromethyl)-1-methylpyrrolidinium chloride is used as a precursor in the synthesis of ionic liquids for their unique properties such as low melting points, high thermal stability, and wide electrochemical windows. These ionic liquids are advantageous in various applications including catalysis, where they can act as solvents or catalysts themselves, and in electrochemistry, where they serve as electrolytes in batteries and fuel cells.
Used in Catalysis:
In the field of catalysis, 2-(chloromethyl)-1-methylpyrrolidinium chloride is used as a component in the preparation of catalytic systems. The resulting ionic liquids can enhance the efficiency of chemical reactions by stabilizing transition states and facilitating selective transformations.
Used in Electrochemistry:
2-(chloromethyl)-1-methylpyrrolidinium chloride contributes to the development of ionic liquids for use in electrochemistry, particularly as electrolytes in energy storage and conversion devices. These ionic liquids offer improved conductivity and stability compared to traditional electrolytes.
Used in Materials Science:
In materials science, 2-(chloromethyl)-1-methylpyrrolidinium chloride is utilized in the creation of innovative materials with tailored properties. The ionic liquids derived from 2-(chloromethyl)-1-methylpyrrolidinium chloride can be engineered to possess specific characteristics, such as self-healing capabilities or enhanced mechanical properties, making them suitable for various high-performance applications.
Used in Pharmaceutical and Biomedical Applications:
Although not explicitly mentioned in the provided materials, given the versatility of ionic liquids, 2-(chloromethyl)-1-methylpyrrolidinium chloride could potentially be used in the pharmaceutical industry for drug solubilization, stabilization, and delivery, as well as in biomedical applications for the design of stimuli-responsive materials.
Check Digit Verification of cas no
The CAS Registry Mumber 54288-69-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,2,8 and 8 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 54288-69:
(7*5)+(6*4)+(5*2)+(4*8)+(3*8)+(2*6)+(1*9)=146
146 % 10 = 6
So 54288-69-6 is a valid CAS Registry Number.
InChI:InChI=1/C6H12ClN.ClH/c1-8-4-2-3-6(8)5-7;/h6H,2-5H2,1H3;1H
54288-69-6Relevant academic research and scientific papers
Benzazepine and benzothiazepine derivatives
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, (2008/06/13)
Vasodilating activity is exhibited by compounds having the formula STR1 wherein X can be --S--or --CH2 --; and R2 is STR2 depending upon the definition of X.
