356537-08-1 Usage
General Description
2-(cyclohex-1-en-1-yl)-N-(4-methoxybenzyl)ethanamine is a chemical compound with a complex molecular structure. It consists of a cyclohexene ring attached to a chain containing an amino group and a benzyl group with a methoxy substituent. 2-(cyclohex-1-en-1-yl)-N-(4-methoxybenzyl)ethanamine is primarily used in research and drug development, particularly in the study of serotonin receptors and related signaling pathways in the brain. Its unique structure and properties make it a valuable tool for understanding the biochemical mechanisms underlying various physiological and pathological processes, including mood regulation, cognition, and neurodegenerative disorders. Additionally, this compound may have potential therapeutic applications in the treatment of psychiatric and neurological conditions, although further research is needed to fully explore its pharmaceutical potential.
Check Digit Verification of cas no
The CAS Registry Mumber 356537-08-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,5,6,5,3 and 7 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 356537-08:
(8*3)+(7*5)+(6*6)+(5*5)+(4*3)+(3*7)+(2*0)+(1*8)=161
161 % 10 = 1
So 356537-08-1 is a valid CAS Registry Number.
356537-08-1Relevant articles and documents
Iron-Catalyzed Reductive Amination of Aldehydes in Isopropyl Alcohol/Water Media as Hydrogen Sources
Petricci, Elena,Santillo, Niccolò,Castagnolo, Daniele,Cini, Elena,Taddei, Maurizio
supporting information, p. 2560 - 2565 (2018/07/29)
Reductive amination can be carried in i-PrOH/H2O as hydrogen sources using commercially available iron carbonyl complexes. Within an aqueous alkaline environment, a hydridocarboferrate is formed and its reducing potential is exploited for hydrogenation of the imine (or iminium ion) obtained in situ from aldehydes or ketones, and primary or secondary amines in almost equimolar ratio. This completely sustainable and hydrogen-free process proceeds at 100 °C using Fe3(CO)12 as catalyst precursor under convectional heating while Fe2(CO)9 gave better results when the reaction was carried out under MW dielectric heating. Both enolizable and non-enolizable aldehydes may be successfully employed in reactions with aliphatic and aromatic amines. (Figure presented.).
