51503-10-7 Usage
Uses
Used in Pharmaceutical Industry:
2-ISOPROPYLPYRROLIDINE is used as a chemical intermediate for the synthesis of various pharmaceuticals, contributing to the development of new drugs and medicines. Its role in this industry is crucial for creating a wide array of therapeutic agents.
Used in Agrochemical Industry:
In the agrochemical sector, 2-ISOPROPYLPYRROLIDINE is utilized as a chemical intermediate, playing a key part in the production of pesticides and other agricultural chemicals that are essential for crop protection and yield enhancement.
Used as a Solvent:
2-ISOPROPYLPYRROLIDINE is employed as a solvent in various chemical processes due to its ability to dissolve a range of substances, facilitating reactions and improving the efficiency of industrial processes.
Used in Polymer Manufacturing:
2-ISOPROPYLPYRROLIDINE is used in the manufacturing of certain polymers, where it contributes to the formation of polymeric materials with specific properties, such as flexibility, strength, or chemical resistance.
Used in Antiviral and Antibacterial Research:
2-ISOPROPYLPYRROLIDINE is used as a subject of study in research for its potential antiviral and antibacterial properties, with the aim of discovering new treatments and preventive measures against infectious diseases.
Check Digit Verification of cas no
The CAS Registry Mumber 51503-10-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,5,0 and 3 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 51503-10:
(7*5)+(6*1)+(5*5)+(4*0)+(3*3)+(2*1)+(1*0)=77
77 % 10 = 7
So 51503-10-7 is a valid CAS Registry Number.
51503-10-7Relevant academic research and scientific papers
A3-coupling reaction as a strategy towards the synthesis of alkaloids
Carmona, Rafaela C.,Wendler, Edison P.,Sakae, George H.,Comassetoa, Jo?o V.,Santos, Alcindo A. Dos
, p. 117 - 123 (2015/02/19)
A number of aldehydes, alkynols and benzylamines were submitted to A3-coupling reaction, under CuCl catalysis, giving strategically functionalized hydroxy-propargylamines. The procedure allows the use of alkyl as well as aryl aldehydes. Representative substrates were converted into five- and six-membered cyclic alkaloids by sequential one-pot N-debenzylation/triple bond reduction promoted by Pd, followed by a Mitsunobu-type cyclization.
