74274-01-4 Usage
Uses
Used in Pharmaceutical Research:
2-(quinolin-2-yl)ethanamine dihydrochloride is used as a reagent in pharmaceutical research for its potential biological activities, particularly as a monoamine oxidase inhibitor. This makes it a promising candidate for the development of new drugs and therapeutic agents for the treatment of various diseases and disorders.
Used in Chemical Research:
In the field of chemical research, 2-(quinolin-2-yl)ethanamine dihydrochloride is used as a reagent to study its structure and properties. Its potential applications in the development of new drugs and therapeutic agents are also being explored, making it a valuable compound for further research and development.
Used in the Treatment of Neurological Conditions:
2-(quinolin-2-yl)ethanamine dihydrochloride is used as a potential pharmacological agent for the treatment of various neurological conditions, such as depression and Parkinson's disease. Its ability to act as a monoamine oxidase inhibitor makes it a promising candidate for the development of new treatments for these conditions.
Used in Drug Development:
Due to its potential biological activities and pharmacological effects, 2-(quinolin-2-yl)ethanamine dihydrochloride is used in the development of new drugs and therapeutic agents. Its structure and properties make it a valuable compound for the creation of innovative treatments for a range of diseases and disorders.
Check Digit Verification of cas no
The CAS Registry Mumber 74274-01-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,2,7 and 4 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 74274-01:
(7*7)+(6*4)+(5*2)+(4*7)+(3*4)+(2*0)+(1*1)=124
124 % 10 = 4
So 74274-01-4 is a valid CAS Registry Number.
74274-01-4Relevant academic research and scientific papers
Synthesis of Bridgehead Nitrogen Heterocycles
Scovill, John P.,Burckhalter, Joseph H.
, p. 23 - 27 (2007/10/02)
Reductive cyclizations of N-imides were accomplished by employing a palladium on carbon catalyst in ethanolic acetic acid as the hydrogenation medium.Reduction of the corresponding N-imides ceased at the 1,2,3,4-tetrahydroquinolyl stage.Controlled reduction of the tetrahydroquinolyl imides with sodium borohydride gave amido alcohols which afforded bridgehead nitrogen heterocycles upon cyclodehydration.
