1241682-49-4 Usage
Uses
Used in Pharmaceutical Research and Drug Development:
(1S)-1-(3-FLUORO-4-METHYLPHENYL)ETHYLAMINE is used as a precursor in the synthesis of pharmaceutical drugs, contributing to the development of new medications with potential therapeutic benefits.
Used in Medicinal Chemistry:
(1S)-1-(3-FLUORO-4-METHYLPHENYL)ETHYLAMINE is utilized as a building block for creating new chemical derivatives, expanding the scope of chemical compounds available for medicinal applications.
Used in Neuroscience Research:
Due to its structural resemblance to other biologically active molecules, (1S)-1-(3-FLUORO-4-METHYLPHENYL)ETHYLAMINE may have potential applications in the field of neuroscience, aiding in the study of brain function and the development of treatments for neurological disorders.
Check Digit Verification of cas no
The CAS Registry Mumber 1241682-49-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,4,1,6,8 and 2 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1241682-49:
(9*1)+(8*2)+(7*4)+(6*1)+(5*6)+(4*8)+(3*2)+(2*4)+(1*9)=144
144 % 10 = 4
So 1241682-49-4 is a valid CAS Registry Number.
1241682-49-4Relevant academic research and scientific papers
Organocatalytic asymmetric biomimetic transamination of aromatic ketone to optically active amine
Xie, Ying,Pan, Hongjie,Xiao, Xiao,Li, Songlei,Shi, Yian
supporting information, p. 8960 - 8962,3 (2012/12/12)
An asymmetric biomimetic transamination of aromatic ketones to optically active amines with o-HOPhCH2NH2 as amine source catalyzed by hydroquinine-derived chiral base is described. Up to 85% ee was obtained.
Organocatalytic asymmetric biomimetic transamination of aromatic ketone to optically active amine
Xie, Ying,Pan, Hongjie,Xiao, Xiao,Li, Songlei,Shi, Yian
supporting information, p. 8960 - 8962 (2013/01/15)
An asymmetric biomimetic transamination of aromatic ketones to optically active amines with o-HOPhCH2NH2 as amine source catalyzed by hydroquinine-derived chiral base is described. Up to 85% ee was obtained.
