1228570-26-0 Usage
General Description
(S)-2-(4-(trifluoromethyl)phenyl)piperidine is a chemical compound with the molecular formula C15H17F3N. It is a piperidine derivative with a trifluoromethyl substituent attached to the phenyl group. (S)-2-(4-(TRIFLUOROMETHYL)PHENYL)PIPERIDINE is of interest in pharmaceutical and medicinal chemistry due to its potential use as a building block or intermediate in the synthesis of various biologically active molecules. The trifluoromethyl group, with its unique electronic and steric properties, can impart desirable characteristics to the molecules it is incorporated into, making (S)-2-(4-(trifluoromethyl)phenyl)piperidine a valuable building block for the generation of novel pharmaceuticals and bioactive compounds. Its specific applications may include drug discovery, agrochemical development, and materials science.
Check Digit Verification of cas no
The CAS Registry Mumber 1228570-26-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,2,8,5,7 and 0 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1228570-26:
(9*1)+(8*2)+(7*2)+(6*8)+(5*5)+(4*7)+(3*0)+(2*2)+(1*6)=150
150 % 10 = 0
So 1228570-26-0 is a valid CAS Registry Number.
1228570-26-0Relevant articles and documents
Amine-promoted asymmetric (4+2) annulations for the enantioselective synthesis of tetrahydropyridines: A traceless and recoverable auxiliary strategy
Hu, Pengfei,Hu, Jian,Jiao, Jiajun,Tong, Xiaofeng
, p. 5319 - 5322 (2013/06/05)
Gone, without a trace: The in situ reaction of 2-(acetoxymethyl)buta-2,3- dienoate and a secondary amine produces a 2-methylene-3-oxobutanoate equivalent that can be used in asymmetric [4+2] annulations with N-tosylimines to provide tetrahydropyridines in
