180683-45-8 Usage
Uses
Used in Medicinal Chemistry:
(S)-1-(2-Hydroxy-3-methylphenyl)ethylamine is used as a key intermediate in the synthesis of various pharmaceutical compounds for its ability to interact with neurotransmitter receptors in the central nervous system. This interaction makes it a promising candidate for the development of drugs targeting neurological disorders and mental health conditions.
Used in Drug Development:
In the pharmaceutical industry, (S)-1-(2-Hydroxy-3-methylphenyl)ethylamine is utilized as a building block for the creation of novel drugs. Its chiral nature allows for the exploration of stereoselective synthesis, which can lead to more effective and safer medications with fewer side effects.
Used in Neurological Research:
(S)-1-(2-Hydroxy-3-methylphenyl)ethylamine is employed as a research tool in the study of neurological disorders and mental health conditions. Its psychoactive effects and interaction with neurotransmitter receptors provide insights into the underlying mechanisms of these conditions, aiding in the development of targeted therapies.
Used in Biochemical Processes:
This chiral amine is involved in various biochemical processes within the body, making it an important compound for understanding and modulating these pathways. Its role in biochemical processes further underscores its potential as a therapeutic agent in the treatment of various diseases and conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 180683-45-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,0,6,8 and 3 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 180683-45:
(8*1)+(7*8)+(6*0)+(5*6)+(4*8)+(3*3)+(2*4)+(1*5)=148
148 % 10 = 8
So 180683-45-8 is a valid CAS Registry Number.
180683-45-8Relevant academic research and scientific papers
Chiral phosphoric acid-catalyzed enantioselective transfer hydrogenation of ortho-hydroxyaryl alkyl N - H ketimines
Nguyen, Thanh Binh,Bousserouel, Hadjira,Wang, Qian,Gueritte, Francoise
supporting information; experimental part, p. 4705 - 4707 (2010/12/24)
The first enantioselective chiral phosphoric acid-catalyzed transfer hydrogenation of unprotected ortho-hydroxyaryl alkyl N - H ketimines using Hantszch di-tert-butyl ester as a reductant is reported. A variety of ortho-hydroxybenzylamines were obtained in good to excellent yields and enantiomeric excesses.
