1212107-18-0 Usage
Description
(1R)-1-(4-BUTYLPHENYL)ETHANAMINE, also known as 4-butyl-1-phenylethylamine, is a chiral amine with the molecular formula C12H19N. It is a chemical compound that has a specific orientation of its atoms, which makes it unique in its properties and applications.
Uses
Used in Scientific Research:
(1R)-1-(4-BUTYLPHENYL)ETHANAMINE is used as a precursor in the synthesis of other chemicals, playing a crucial role in the development of new compounds for various purposes.
Used in Pharmaceutical Production:
(1R)-1-(4-BUTYLPHENYL)ETHANAMINE serves as a starting material in the production of pharmaceutical drugs, contributing to the creation of medications that can address a range of health issues.
Used in Psychoactive Drug Development:
As a psychoactive drug, (1R)-1-(4-BUTYLPHENYL)ETHANAMINE affects the central nervous system and is used in research for its potential therapeutic applications in treating conditions such as depression and ADHD.
Used in Neurodegenerative Disease Treatment:
(1R)-1-(4-BUTYLPHENYL)ETHANAMINE has been researched for its potential use as a dopaminergic agent, making it a candidate for the treatment of Parkinson's disease and potentially offering new therapeutic options for patients.
Check Digit Verification of cas no
The CAS Registry Mumber 1212107-18-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,1,2,1,0 and 7 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1212107-18:
(9*1)+(8*2)+(7*1)+(6*2)+(5*1)+(4*0)+(3*7)+(2*1)+(1*8)=80
80 % 10 = 0
So 1212107-18-0 is a valid CAS Registry Number.
1212107-18-0Relevant articles and documents
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.
