123982-91-2 Usage
Uses
Used in Pharmaceutical Applications:
(R)-1-(2-benzyloxyphenyl)ethylamine hydrochloride is used as an intermediate in the synthesis of various pharmaceutical compounds for [application reason]. Its amine structure and hydrochloride salt form make it a versatile building block in the development of new drugs.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, (R)-1-(2-benzyloxyphenyl)ethylamine hydrochloride is used as a research compound for [application reason]. Its unique structure allows scientists to study its interactions with biological targets and evaluate its potential as a therapeutic agent.
Used in Neuroscience Research:
(R)-1-(2-benzyloxyphenyl)ethylamine hydrochloride is also used in neuroscience research as a chemical probe for [application reason]. Its ability to modulate specific receptors or enzymes in the nervous system can provide valuable insights into the underlying mechanisms of various neurological disorders and potential treatment strategies.
Used in Chemical Synthesis:
In the chemical synthesis industry, (R)-1-(2-benzyloxyphenyl)ethylamine hydrochloride is used as a reagent or catalyst for [application reason]. Its unique properties enable it to facilitate specific chemical reactions, leading to the production of desired compounds with high efficiency and selectivity.
Check Digit Verification of cas no
The CAS Registry Mumber 123982-91-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,3,9,8 and 2 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 123982-91:
(8*1)+(7*2)+(6*3)+(5*9)+(4*8)+(3*2)+(2*9)+(1*1)=142
142 % 10 = 2
So 123982-91-2 is a valid CAS Registry Number.
123982-91-2Relevant academic research and scientific papers
Enantiopure Ti(IV) amino triphenolate complexes as NMR chiral solvating agents
Zonta, Cristiano,Kolarovic, Andrej,Mba, Miriam,Pontini, Marta,KUendig, E. Peter,Licini, Giulia
experimental part, p. 796 - 800 (2012/01/19)
Enantiopure Ti(IV) complexes bearing pseudo-C3 amino triphenolate ligands have been synthesized and characterized. The complexes bearing ortho phenyl groups act as 1H NMR chiral solvating agent (CSA) for the stereochemical analysis of a series of sulfoxides. The coordination of a Lewis base coligand (sulfoxide) and the presence of aromatic rings are the key structural factors for the efficiency of the CSA. Chirality, 2011. 2011 Wiley-Liss, Inc. Copyright
