135540-11-3 Usage
Description
1-(Chloro-1-pyrrolidinylmethylene)pyrrolidinium hexafluorophosphate is a white solid chemical compound that serves as a versatile reagent in various chemical reactions and processes. It is known for its ability to facilitate enantioselective desymmetrization of meso-aziridines, promote peptide coupling, and act as a reagent in the heterocycle formation of chloroformamidinium salts. Additionally, it is utilized in the oxidative insertion process for the synthesis of palladium and nickel catalysts.
Uses
Used in Enantioselective Desymmetrization of meso-aziridines:
1-(Chloro-1-pyrrolidinylmethylene)pyrrolidinium hexafluorophosphate is used as a reagent for the enantioselective desymmetrization of meso-aziridines, enabling the formation of chiral products with high selectivity and efficiency.
Used in Peptide Coupling:
In the pharmaceutical and biotechnology industries, 1-(Chloro-1-pyrrolidinylmethylene)pyrrolidinium hexafluorophosphate is used as a coupling agent to facilitate the formation of peptide bonds, which is crucial for the synthesis of various peptides and proteins.
Used in Heterocyclization of chloroformamidinium salts:
1-(Chloro-1-pyrrolidinylmethylene)pyrrolidinium hexafluorophosphate is used as a reagent in the heterocyclization process of chloroformamidinium salts, which is an important step in the synthesis of various heterocyclic compounds with potential applications in pharmaceuticals, agrochemicals, and materials science.
Used in Oxidative Insertion for Palladium and Nickel Catalyst Synthesis:
In the field of catalysis, 1-(Chloro-1-pyrrolidinylmethylene)pyrrolidinium hexafluorophosphate is employed as a reagent for oxidative insertion, which is a key step in the synthesis of palladium and nickel catalysts. These catalysts are widely used in various chemical reactions, including cross-coupling reactions, hydrogenations, and C-H activation processes.
Used in Chemical Synthesis:
1-(Chloro-1-pyrrolidinylmethylene)pyrrolidinium hexafluorophosphate is used as a versatile reagent in various chemical synthesis processes across different industries, such as pharmaceuticals, agrochemicals, and materials science, due to its ability to promote selective reactions and improve product yields.
Check Digit Verification of cas no
The CAS Registry Mumber 135540-11-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,5,5,4 and 0 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 135540-11:
(8*1)+(7*3)+(6*5)+(5*5)+(4*4)+(3*0)+(2*1)+(1*1)=103
103 % 10 = 3
So 135540-11-3 is a valid CAS Registry Number.
