1015242-07-5 Usage
General Description
2-(Pyrrolidin-1-yl)pyrimidine-5-boronic acid pinacol ester is a chemical compound that principally belongs to the class of organic compounds known as pyrimidines and pyrimidine derivatives. These are compounds that contain a pyrimidine ring, which is a six-member aromatic heterocycle, made up of two nitrogen atoms and four carbon atoms. The specific compound, 2-(Pyrrolidin-1-yl)pyrimidine-5-boronic acid pinacol ester, incorporates additional elements and structures including the nitrogen-containing five-member pyrrolidine ring and a boronic acid pinacol ester. While its use is not widely specified, pyrimidine derivatives are generally utilized in a range of pharmaceutical and therapeutic applications, and boronic acids and their esters are often used in organic chemistry and molecular biology processes.
Check Digit Verification of cas no
The CAS Registry Mumber 1015242-07-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,1,5,2,4 and 2 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1015242-07:
(9*1)+(8*0)+(7*1)+(6*5)+(5*2)+(4*4)+(3*2)+(2*0)+(1*7)=85
85 % 10 = 5
So 1015242-07-5 is a valid CAS Registry Number.
InChI:InChI=1S/C14H22BN3O2/c1-13(2)14(3,4)20-15(19-13)11-9-16-12(17-10-11)18-7-5-6-8-18/h9-10H,5-8H2,1-4H3
1015242-07-5Relevant articles and documents
Two Ligands Transfer from Ag to Pd: En Route to (SIPr)Pd(CF2H)(X) and Its Application in One-Pot C-H Borylation/Difluoromethylation
Herbert, Simon,Kinzel, Tom,Shen, Qilong,Zhang, Wei,Zhao, Haiwei
, p. 3596 - 3604 (2020)
A process for the concurrent transfer of both the NHC ligand and the difluoromethyl group from [(SIPr)Ag(CF2H)] to PdX2 (X = Cl, OAc, and OPiv) for the preparation of [(SIPr)Pd(CF2H)X] complexes is described. These complexes were air-stable and easily underwent transmetalation with aryl pinacol boronate/reductive elimination to generate ArCF2H in high yields. Based on this discovery, the first one-pot C-H borylation and difluoromethylation process for the preparation of difluoromethylated (hetero)arenes was developed.
