128495-49-8Relevant academic research and scientific papers
Fluorine substituted methoxyphenylalkyl amides as potent melatonin receptor agonists?
Tsotinis, Andrew,Kompogennitaki, Rodanthi,Papanastasiou, Ioannis,Garratt, Peter J.,Bocianowska, Alina,Sugden, David
supporting information, p. 460 - 464 (2019/05/29)
A series of fluorine substituted methoxyphenylalkyl amides were prepared with different orientations of the fluorine and methoxy groups with respect to the alkylamide side chain and with alkyl sides of differing lengths (n = 1-3). β-Dimethyl and α-methyl
Synthesis and Dopamine Receptor Affinities of 2-(4-fluoro-3-hydroxyphenyl)ethylamine and N-Substituted Derivatives
Claudi, Francesco,Cardellini, Mario,Cingolani, Gian Mario,Piergentili, Alessandro,Pertuzzi, Guidubaldo,Balduini, Walter
, p. 2408 - 2412 (2007/10/02)
The synthesis of 2-(4-fluoro-3-hydroxyphenyl)ethylamine (26) and of some N,N-dialkyl derivatives (27-30) starting from 4-fluoro-3-hydroxytoluene and their in vitro binding affinities for dopamine (DA) receptor are reported.The amine 26 can be regarded as
