10132-28-2 Usage
General Description
2-(butylamino)pyrimidine is a chemical compound with the molecular formula C9H14N4. It is a pyrimidine derivative that contains a butylamino group attached to the second carbon atom of the pyrimidine ring. It is commonly used as an intermediate in the synthesis of pharmaceuticals, agrochemicals, and other organic compounds. 2-(butylamino)pyrimidine has the potential to act as a nucleoside analog, making it useful in the development of antiviral and anticancer drugs. Additionally, 2-(butylamino)pyrimidine has been studied for its potential biological activities, including its effects on cell growth and proliferation. Overall, this chemical compound has a range of potential applications in the field of pharmaceutical and agrochemical research.
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 articles and documents
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.