648424-43-5 Usage
Uses
Used in Electrochemical Systems:
1-Hexyl-3-Methylimidazolium Perchlorate is used as an electrolyte in electrochemical systems for its ability to improve the performance and stability of these systems.
Used in Organic Synthesis:
1-Hexyl-3-Methylimidazolium Perchlorate is used as a solvent in organic synthesis due to its favorable properties, which can enhance the efficiency and selectivity of chemical reactions.
Used in Materials Processing:
1-Hexyl-3-Methylimidazolium Perchlorate is used as a processing aid in materials processing to facilitate the handling and manipulation of various materials.
Used in Lubrication:
1-Hexyl-3-Methylimidazolium Perchlorate is used as a lubricant in industrial applications, taking advantage of its thermal stability and non-flammability to improve the performance of mechanical systems.
Used in Nuclear Fuel Recycling:
1-Hexyl-3-Methylimidazolium Perchlorate is used in the recycling of nuclear fuel, where its chemical properties can contribute to the efficiency and safety of the process.
Note: The environmental impact and toxicity of 1-Hexyl-3-Methylimidazolium Perchlorate are subjects of ongoing research, which may influence its applications and use in the future.
Check Digit Verification of cas no
The CAS Registry Mumber 648424-43-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,4,8,4,2 and 4 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 648424-43:
(8*6)+(7*4)+(6*8)+(5*4)+(4*2)+(3*4)+(2*4)+(1*3)=175
175 % 10 = 5
So 648424-43-5 is a valid CAS Registry Number.
648424-43-5Relevant articles and documents
Thermodynamic and molecular origin of interfacial rate enhancements and endo -selectivities of a Diels-Alder reaction
Beniwal, Vijay,Kumar, Anil
, p. 4297 - 4306 (2017/08/14)
Organic reactions in general display large rate accelerations when performed under interfacial conditions, such as on water or at ionic liquid interfaces. However, a clear picture of the physicochemical factors responsible for this large rate enhancements is not available. To gain an understanding of the thermodynamic and molecular origin of these large rate enhancements, we performed a Diels-Alder reaction between cyclopentadiene and methyl acrylate at ionic liquid/n-hexane interfaces. This study describes, for the first time, a methodology for the calculation of the activation parameters of an interfacial reaction. It has been seen that the energy of activation for an interfacial reaction is much smaller than that of the corresponding homogeneous reaction, resulting into the large rate acceleration for the interfacial reaction. Furthermore, the study describes the effects of the alkyl chain length of ionic liquid cations, the extent of heterogeneity, and the polarity of ionic liquids on the rate constants and stereoselectivity of the reaction.
Synthesis of methyl orange using ionic liquids
Astolfi, Danette L.,Mayville, Francis C.
, p. 9223 - 9224 (2007/10/03)
Two ionic liquids were synthesized, each system consisting of the 1-hexyl-3-methylimidazolium ion ([hmim]+) as the cation and either hexafluorophosphate ([PF6]-), or perchlorate ([ClO4]-) as the anions. This study involves
