148065-53-6 Usage
Uses
Used in Pharmaceutical Industry:
(S)-1-(Anthracen-10-yl)ethanamine is used as an intermediate in the synthesis of various pharmaceuticals. Its unique structure and functional groups make it a valuable building block for the development of new drugs with potential therapeutic applications.
Used in Dye and Fluorescent Dye Production:
(S)-1-(Anthracen-10-yl)ethanamine is used as a key component in the production of dyes and fluorescent dyes. Its anthracene core provides characteristic optical properties, making it suitable for use in various applications, such as in the textile industry, as a tracer in biological research, or in the development of sensors.
Used in Organic Synthesis:
(S)-1-(Anthracen-10-yl)ethanamine serves as a versatile building block in organic synthesis. Its amine group can be further functionalized, allowing for the creation of a wide range of chemical compounds with diverse properties and applications.
Used in Anti-Cancer Research:
(S)-1-(Anthracen-10-yl)ethanamine has shown potential as an anti-cancer agent. Its unique structure and biological activity make it a promising candidate for the development of new cancer therapies. Further research is needed to fully understand its mechanism of action and optimize its potential as a cancer treatment.
Used in Coordination Chemistry:
(S)-1-(Anthracen-10-yl)ethanamine can act as a ligand in coordination chemistry, forming complexes with various metal ions. These complexes can exhibit unique properties, such as catalytic activity or magnetic behavior, making them valuable in the development of new materials and catalysts.
Check Digit Verification of cas no
The CAS Registry Mumber 148065-53-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,8,0,6 and 5 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 148065-53:
(8*1)+(7*4)+(6*8)+(5*0)+(4*6)+(3*5)+(2*5)+(1*3)=136
136 % 10 = 6
So 148065-53-6 is a valid CAS Registry Number.
148065-53-6Relevant articles and documents
Asymmetric synthesis of 1-(9-anthracenyl)ethylamine and its trifluoromethyl analogue via nucleophilic addition to an N -(tert -butylsulfinyl)imine
Hernandez-Rodriguez, Marcos,Castillo-Hernandez, Tania,Trejo-Huizar, Karla Elisa
, p. 2817 - 2821 (2011)
Asymmetric synthesis of the 9-anthracenyl analogues of 1-phenylethylamine and 2,2,2-trifluoro-1-phenylethylamine was achieved via nucleophilic addition to the corresponding N-(tert-butylsulfinyl)imine. Georg Thieme Verlag Stuttgart, New York.
Chromatographic resolution of anthryl- and phenathryl-ethylamines and their use as chiral modifiers for catalytic heterogeneous hydrogenation of ethyl pyruvate
Solladie-Cavallo,Marsol,Suteu,Garin
, p. 245 - 249 (2007/10/03)
Efficient synthesis (1 to 2 steps and 95-97% overall yields) and efficient chiral chromatographic resolution of rac-anthryl-ethylamine (6a) and phenanthryl-ethylamine (7a) (35-38% of each enantiomers) have been performed. Tested as chiral modifiers for catalytic heterogeneous hydrogenation of ethyl pyruvate, (+)-6a and (+)-7a led to 12-30% ee and the monobenzyl derivative (-)-7b provided 40% ee.
