339017-83-3 Usage
General Description
6-Chloro-N-ethyl-2-(methylsulfanyl)-4-pyrimidinamine is a chemical compound characterized by a specific structure and certain chemical properties. Notably, it has one nitrogen atom, one sulfur atom, two carbon atoms, and a chlorine atom in its chemical composition. As the name suggests, it has chlorine and methylsulfanyl as functional groups. It is derived from a pyrimidine, which is a basic aromatic ring consisting of four carbon atoms and two nitrogen atoms. The 'amine' in its name implies the presence of an amine group (-NH2), which is an important functional group in the chemistry of organic compounds. This chemical can be used in a variety of applications, but its specific usage can vary depending on factors like its purity and the presence of other elements or chemicals. However, details about its exact applications or safety measures need more substantial data and research.
Check Digit Verification of cas no
The CAS Registry Mumber 339017-83-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,3,9,0,1 and 7 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 339017-83:
(8*3)+(7*3)+(6*9)+(5*0)+(4*1)+(3*7)+(2*8)+(1*3)=143
143 % 10 = 3
So 339017-83-3 is a valid CAS Registry Number.
339017-83-3Relevant articles and documents
Discovery of High-Affinity Inhibitors of the BPTF Bromodomain
Lu, Tian,Lu, Haibo,Duan, Zhe,Wang, Jun,Han, Jie,Xiao, Senhao,Chen, HuanHuan,Jiang, Hao,Chen, Yu,Yang, Feng,Li, Qi,Chen, Dongying,Lin, Jin,Li, Bo,Jiang, Hualiang,Chen, Kaixian,Lu, Wenchao,Lin, Hua,Luo, Cheng
, p. 12075 - 12088 (2021/09/02)
The dysfunctional bromodomain PHD finger transcription factor (BPTF) exerts a pivotal influence in the occurrence and development of many human diseases, particularly cancers. Herein, through the structural decomposition of the reported BPTF inhibitor TP-
Identification of aminopyrimidine regioisomers via line broadening effects in1H and13C NMR spectroscopy
Garner, James,Hill, Tim,Odell, Luke,Keller, Paul,Morgan, Jody,McCluskey, Adam
, p. 1079 - 1083 (2007/10/03)
Substituted mono- and diamino-pyrimidines were synthesized as part of our medicinal chemistry programmes. Primary amines substituted at the 4-position exhibited room-temperature line broadening effects in both 1H and 13C NMR spectros
