68985-04-6 Usage
Uses
Used in Cardiovascular Medicine:
(+)-Metoprolol hydrochloride is used as an antihypertensive agent for the treatment of high blood pressure. It helps to lower the heart rate and blood pressure, thereby reducing the strain on the heart and managing hypertension effectively.
(+)-Metoprolol hydrochloride is also used as an anti-anginal medication to alleviate chest pain (angina) by reducing the workload on the heart and improving blood flow to the heart muscles.
Used in Cardiology:
(+)-Metoprolol hydrochloride is utilized as an anti-arrhythmic agent for the management of heart rhythm disorders. It helps to regulate the heart's electrical activity, ensuring a more stable and regular heartbeat.
(+)-Metoprolol hydrochloride is used as a preventive measure for patients who have previously experienced a heart attack. It helps to reduce the risk of future heart attacks by maintaining a lower heart rate and blood pressure, thus protecting the heart from additional strain.
Common side effects of (+)-Metoprolol hydrochloride include dizziness, fatigue, and slow heart rate. However, its benefits in managing cardiovascular conditions often outweigh these temporary side effects, making it a widely prescribed medication in the field of cardiology.
Check Digit Verification of cas no
The CAS Registry Mumber 68985-04-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,8,9,8 and 5 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 68985-04:
(7*6)+(6*8)+(5*9)+(4*8)+(3*5)+(2*0)+(1*4)=186
186 % 10 = 6
So 68985-04-6 is a valid CAS Registry Number.
68985-04-6Relevant academic research and scientific papers
Sukuraba,Takahashi,Takeda,Achiwa
, p. 738 - 747 (1995)
The complexes of pyrrolidine bisphosphine ligands (CPMs) with rhodium (I) were found to be efficient catalysts for asymmetric hydrogenation of α-amino ketone hydrochloride derivatives. Utilizing this methodology, we have developed efficient asymmetric syntheses of the optically active β-amino alcohols, phenylephrine, levamisole, carnitine and propranolol.