10132-28-2 Usage
Uses
Used in Pharmaceutical Industry:
2-(Butylamino)pyrimidine is used as a chemical intermediate for the synthesis of various pharmaceuticals, leveraging its structural properties to contribute to the development of new drugs.
Used in Agrochemical Industry:
In the agrochemical sector, 2-(Butylamino)pyrimidine serves as an intermediate in the creation of compounds that address agricultural needs, such as pest control and crop protection.
Used in Antiviral and Anticancer Drug Development:
2-(Butylamino)pyrimidine is utilized as a nucleoside analog in the research and development of antiviral and anticancer medications, due to its potential to interfere with viral and cancerous cell replication processes.
Used in Biological Research:
2-(butylamino)pyrimidine is applied in biological studies to investigate its effects on cell growth and proliferation, providing insights into its possible role in therapeutic applications.
Check Digit Verification of cas no
The CAS Registry Mumber 10132-28-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,1,3 and 2 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 10132-28:
(7*1)+(6*0)+(5*1)+(4*3)+(3*2)+(2*2)+(1*8)=42
42 % 10 = 2
So 10132-28-2 is a valid CAS Registry Number.
10132-28-2Relevant academic research and scientific papers
Ruthenium-Catalyzed Reductive Arylation of N-(2-Pyridinyl)amides with Isopropanol and Arylboronate Esters
Ronson, Thomas O.,Renders, Evelien,Van Steijvoort, Ben F.,Wang, Xubin,Wybon, Clarence C. D.,Prokopcová, Hana,Meerpoel, Lieven,Maes, Bert U. W.
supporting information, p. 482 - 487 (2019/01/04)
A new three-component reductive arylation of amides with stable reactants (iPrOH and arylboronate esters), making use of a 2-pyridinyl (Py) directing group, is described. The N-Py-amide substrates are readily prepared from carboxylic acids and PyNH2, and the resulting N-Py-1-arylalkanamine reaction products are easily transformed into the corresponding chlorides by substitution of the HN-Py group with HCl. The 1-aryl-1-chloroalkane products allow substitution and cross-coupling reactions. Therefore, a general protocol for the transformation of carboxylic acids into a variety of functionalities is obtained. The Py-NH2 by-product can be recycled.
