1017234-23-9 Usage
Description
(1S)-N-((S)-1-(3-hydroxyphenyl)ethyl)-N-methyl-1-phenylethanamine, also known as L-Adrenaline, is a synthetic compound with significant pharmacological effects. It is a sympathomimetic amine that functions as a neurotransmitter in the body, playing a key role in the "fight or flight" response. L-Adrenaline is a potent stimulant of the adrenergic receptors, which results in increased heart rate, blood pressure, and bronchodilation.
Uses
Used in Medical Treatments:
L-Adrenaline is utilized as a medical treatment for severe allergic reactions, where it helps to counteract the symptoms of anaphylaxis by increasing blood flow and reducing the severity of the allergic response.
Used in Cardiac Arrest Management:
In cases of cardiac arrest, L-Adrenaline is used to stimulate the heart and improve the chances of restoring a regular heartbeat.
Used as a Bronchodilator in Asthma Treatment:
L-Adrenaline is employed as a bronchodilator in asthma treatment, helping to relax the muscles around the airways and alleviate breathing difficulties.
Check Digit Verification of cas no
The CAS Registry Mumber 1017234-23-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,1,7,2,3 and 4 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1017234-23:
(9*1)+(8*0)+(7*1)+(6*7)+(5*2)+(4*3)+(3*4)+(2*2)+(1*3)=99
99 % 10 = 9
So 1017234-23-9 is a valid CAS Registry Number.
1017234-23-9Relevant articles and documents
General strategy for large-scale synthesis of (+)-rivastigmine and (+)-NPS R-568
Rao, Ramakrishna,Shewalkar, Mukesh Padmakar,Nandipati, Ramadevi,Yadav, Jhillu Singh,Khagga, Mukkanti,Shinde, Devanand Baburao
, p. 589 - 598 (2011/11/29)
An economically viable strategy for the total synthesis of (+)-rivastigmine and (+)-NPS R-568 has been reported. The strategy involves regioselective hydrogenation of diastereomerically pure bis amine to realize the desired a-methyl chiral substituted benzyl amine. The route is economical, scalable, and versatile enough to be adapted to similar classes of compounds. Taylor & Francis Group, LLC.
Novel convenient synthesis of rivastigmine
Hu, Meng,Zhang, Fu-Li,Xie, Mei-Hua
experimental part, p. 1527 - 1533 (2009/10/17)
A novel and convenient synthesis of rivastigmine has been reported. This procedure provides high yield and excellent enantiomeric excess (100% ee) starting from the diastereromerically pure (S)-1-(3-methoxyphenyl)-N-[(S)-1- phenylethyl] ethanamine. Copyright Taylor & Francis Group, LLC.
