1228570-26-0 Usage
Uses
Used in Pharmaceutical and Medicinal Chemistry:
(S)-2-(4-(TRIFLUOROMETHYL)PHENYL)PIPERIDINE is used as a building block for the synthesis of biologically active molecules due to its unique electronic and steric properties imparted by the trifluoromethyl group.
Used in Drug Discovery:
(S)-2-(4-(TRIFLUOROMETHYL)PHENYL)PIPERIDINE is used as an intermediate in drug discovery, where its incorporation into various molecules can lead to the development of new pharmaceuticals with improved characteristics.
Used in Agrochemical Development:
(S)-2-(4-(TRIFLUOROMETHYL)PHENYL)PIPERIDINE is used as a component in the development of agrochemicals, potentially enhancing the effectiveness of these compounds in agricultural applications.
Used in Materials Science:
(S)-2-(4-(TRIFLUOROMETHYL)PHENYL)PIPERIDINE is utilized in materials science for the creation of novel materials with specific properties, taking advantage of the compound's unique structural features.
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
Applications of N′-alkylated derivatives of TsDPEN in the asymmetric transfer hydrogenation of C=O and C=N bonds
Martins, Jose E.D.,Contreras Redondo, Miguel A.,Wills, Martin
experimental part, p. 2258 - 2264 (2010/11/03)
Arene/Ru(II) complexes of (R,R)-N-alkyl-TsDPEN ligands are effective in the asymmetric transfer hydrogenation of ketones and imines in formic acid/triethylamine solution. The complex derived from the N′-Bn derivative of TsDPEN reduces monocyclic imines in up to 60% ee, whilst the N′-Me derivative of TsDPEN forms a more active catalyst than the non-alkylated analogue and reduces ketones in up to 97% ee.
