81947-89-9 Usage
Type of Drug
Beta-blocker medication
Purpose
Treats high blood pressure, improves survival after a heart attack, and prevents migraine headaches
Mechanism of Action
Blocks the action of certain natural substances (e.g., epinephrine) on the heart and blood vessels, lowering blood pressure and decreasing the workload on the heart
Administration
Usually taken by mouth
Side Effects
Dizziness, fatigue, and difficulty sleeping
Precaution
Follow dosage instructions provided by a healthcare professional
Chemical Structure
Contains a tert-butylamino group, a phenoxy group connected to a 6-chloropyridazin-3-yl group, and a secondary alcohol (-OH) group
Molecular Weight
Approximately 361.86 g/mol
Appearance
Nebivolol is a white to off-white crystalline powder
Solubility
Soluble in ethanol, slightly soluble in water, and practically insoluble in heptane
Stability
Stable under normal temperature and pressure conditions, but should be stored in a tight, light-resistant container
Drug Interactions
May interact with other medications, including other beta-blockers, calcium channel blockers, and certain antidepressants
Breastfeeding
It is unknown whether nebivolol passes into breast milk, so caution should be exercised when administered to nursing mothers
Metabolism
Metabolized in the liver by the cytochrome P450 system, primarily by the CYP2D6 enzyme
Excretion
Eliminated primarily in the urine, with a smaller portion excreted in the feces
Half-life
Approximately 12-24 hours in healthy adults
Check Digit Verification of cas no
The CAS Registry Mumber 81947-89-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,9,4 and 7 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 81947-89:
(7*8)+(6*1)+(5*9)+(4*4)+(3*7)+(2*8)+(1*9)=169
169 % 10 = 9
So 81947-89-9 is a valid CAS Registry Number.
InChI:InChI=1/C17H22ClN3O2/c1-17(2,3)19-10-12(22)11-23-15-7-5-4-6-13(15)14-8-9-16(18)21-20-14/h4-9,12,19,22H,10-11H2,1-3H3
81947-89-9Relevant articles and documents
PROCESS FOR PREPARING 3-CHLORO-6-(2-HYDROXYPHENYL)-PYRIDAZINES
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, (2008/06/13)
A process for preparing 3-chloro-6-(2-hydroxyphenyl) pyridazines by the reaction of 6-(2-hydroxyphenyl)-3(2H)-pyridazinones with phosphorus oxychloride and a disubstituted formamide. The chloropyridazine compounds are useful intermediates for preparing co