143063-66-5 Usage
General Description
BENZYL-(1-NAPHTHALEN-2-YL-ETHYL)-AMINE, also known as N-(2-(Benzylamino)ethyl)-2-naphthylamine, is a chemical compound with the molecular formula C23H22N. It is a member of the amine class and has a benzyl group attached to an ethyl chain, which in turn is connected to a 1-naphthyl group. BENZYL-(1-NAPHTHALEN-2-YL-ETHYL)-AMINE has applications in the fields of pharmaceuticals, organic synthesis, and chemical research. It is commonly used as a precursor in the synthesis of various organic compounds and as a building block for the development of new chemical entities. The detailed properties, uses, and potential hazards of BENZYL-(1-NAPHTHALEN-2-YL-ETHYL)-AMINE should be thoroughly researched and understood before handling or using this chemical.
Check Digit Verification of cas no
The CAS Registry Mumber 143063-66-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,3,0,6 and 3 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 143063-66:
(8*1)+(7*4)+(6*3)+(5*0)+(4*6)+(3*3)+(2*6)+(1*6)=105
105 % 10 = 5
So 143063-66-5 is a valid CAS Registry Number.
143063-66-5Relevant articles and documents
L-Valine derived chiral N-sulfinamides as effective organocatalysts for the asymmetric hydrosilylation of N-alkyl and N-aryl protected ketimines
Wang, Chao,Wu, Xinjun,Zhou, Li,Sun, Jian
, p. 577 - 582 (2015/02/02)
l-Valine derived N-sulfinamides have been developed as efficient enantioselective Lewis basic organocatalysts for the asymmetric reduction of N-aryl and N-alkyl ketimines with trichlorosilane. Catalyst 3c afforded up to 99% yield and 96% ee in the reduction of N-alkyl ketimines and up to 98% yield and 98% ee in the reduction of N-aryl ketimines.
Asymmetric titanocene-catalyzed hydrogenation of imines
Willoughby, Christopher A.,Buchwald, Stephen L.
, p. 7562 - 7564 (2007/10/02)
-
