25354-42-1 Usage
Uses
Used in Organic Synthesis:
Methanesulfonic acid, trifluoro-, cyclopropyl ester is used as a reagent in organic synthesis for its high reactivity, enabling the formation of various complex organic compounds.
Used in Chemical Reactions as a Strong Acid Catalyst:
In the chemical industry, Methanesulfonic acid, trifluoro-, cyclopropyl ester is utilized as a strong acid catalyst to accelerate various chemical reactions, enhancing the reaction rates and improving the overall efficiency of the process.
Used as a Solvent in Chemical Processes:
Methanesulfonic acid, trifluoro-, cyclopropyl ester serves as a solvent in certain chemical processes, facilitating the dissolution of specific substances and promoting the desired chemical reactions.
Used as a Polymer Stabilizer:
In the polymer industry, Methanesulfonic acid, trifluoro-, cyclopropyl ester is employed as a stabilizer to enhance the stability and performance of certain types of polymers, ensuring their durability and resistance to degradation.
Check Digit Verification of cas no
The CAS Registry Mumber 25354-42-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,3,5 and 4 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 25354-42:
(7*2)+(6*5)+(5*3)+(4*5)+(3*4)+(2*4)+(1*2)=101
101 % 10 = 1
So 25354-42-1 is a valid CAS Registry Number.
25354-42-1Relevant academic research and scientific papers
Reactions of Cyclopropyl Sulfonates with Nucleophiles: SN2 Displacements at Cyclopropanes with Inversion
Banert, Klaus
, p. 1564 - 1574 (2007/10/02)
Treatment of cyclopropyl trifluoromethanesulfonate (3) with tributylhexadecylphosphonium azide (QN3) in aprotic solvents almost quantitatively afforded cyclopropyl azide (6) in a second-order reaction.Nucleophilic displacements with ring preservation were also achieved using QCN or QBr.The analogous reactions of the epimeric 2-methylcyclopropyl trifluoromethanesulfonates (16, 17) with QN3 highly stereospecifically yielded the 2-methylcyclopropyl azides (24, 25) with inversion in addition to the allylic azides 27, 28, and 29.The product fraction of cyclic azides decrea sed with growing steric hindrance in the order 3 > 16 > 17.The experimental results show that SN2 displacements take place with clean inversion at the cyclopropane carbon atom.
