82572-03-0 Usage
Uses
Used in Pharmaceutical Research and Drug Development:
(R)-1-(Naphthalen-2-yl)ethanamine hydrochloride is used as a chemical compound for its potential therapeutic applications in treating neurological and psychiatric disorders. Its unique properties allow it to be a promising candidate for the development of new drugs targeting these conditions.
Used in Chemical Synthesis:
(R)-1-(Naphthalen-2-yl)ethanamine hydrochloride is used as a chemical intermediate for the synthesis of various organic compounds. Its versatile structure makes it a valuable building block in the creation of new molecules with potential applications in various industries.
Used in Neuroscience Research:
(R)-1-(Naphthalen-2-yl)ethanamine hydrochloride is used as a selective agonist for certain receptors in the central nervous system. This application makes it an important compound in neuroscience research, where it can help scientists better understand the mechanisms of receptor interactions and potentially lead to the development of new treatments for neurological disorders.
Check Digit Verification of cas no
The CAS Registry Mumber 82572-03-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,5,7 and 2 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 82572-03:
(7*8)+(6*2)+(5*5)+(4*7)+(3*2)+(2*0)+(1*3)=130
130 % 10 = 0
So 82572-03-0 is a valid CAS Registry Number.
82572-03-0Relevant academic research and scientific papers
Iridium/monodentate phosphoramidite catalyzed asymmetric hydrogenation of N-aryl imines
Mrsic, Natasa,Minnaard, Adriaan J.,Feringa, Ben L.,Vries, Johannes G. de
supporting information; experimental part, p. 8358 - 8359 (2009/10/23)
(Chemical Equation Presented) Asymmetric hydrogenation of N-aryl acetophenone imines using iridium/PipPhos leads to very high enantioselectivities up to >99percent depending on the presence of electron-donating substituents in the 2-, 3-, and 5-position of the aryl ring. If the substituent is 2-methoxy, the resultant secondary amines are easily oxidatively deprotected using trichloroisocyanuric acid to give the primary amines ingood yield with full retention of enantioselectivity.
Resolution of alpha-(phenoxy) phenylacetic acid derivatives with naphthyl-alkylamines
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Page/Page column 10, (2008/06/13)
The present invention provides a methods and compounds for producing an enantiomerically enriched α-(phenoxy)phenylacetic acid compound of the formula: from a mixture of its enantiomers, where R1 is alkyl or haloalkyl and X is halide.
