926622-53-9 Usage
Description
Benzenemethanamine, a-methyl-2,4,6-tris(1-methylethyl)-, (aS)-, also known as pseudoephedrine, is a medication commonly used as a decongestant for the treatment of nasal congestion, sinus congestion, and Eustachian tube congestion. It works by constricting the blood vessels in the nasal passages, which reduces swelling and allows for easier breathing. Pseudoephedrine is an alphaand beta-adrenergic agonist that also has a mild stimulant effect on the central nervous system.
Uses
Used in Pharmaceutical Industry:
Pseudoephedrine is used as a decongestant for the treatment of nasal congestion, sinus congestion, and Eustachian tube congestion. It is effective in reducing swelling in the nasal passages, allowing for easier breathing.
Used in Over-the-Counter Medications:
Pseudoephedrine is available over-the-counter in many parts of the world, making it accessible for individuals seeking relief from nasal congestion and related symptoms.
Used with Caution in Individuals with Certain Health Conditions:
Pseudoephedrine should be used with caution in individuals with high blood pressure, heart disease, or thyroid disease, as it can cause side effects such as increased blood pressure, insomnia, and dizziness.
Regulated in Some Countries:
Due to its potential for being used in the illicit production of methamphetamine, the sale and use of pseudoephedrine are regulated in some countries to prevent misuse.
Check Digit Verification of cas no
The CAS Registry Mumber 926622-53-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,2,6,6,2 and 2 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 926622-53:
(8*9)+(7*2)+(6*6)+(5*6)+(4*2)+(3*2)+(2*5)+(1*3)=179
179 % 10 = 9
So 926622-53-9 is a valid CAS Registry Number.
926622-53-9Relevant articles and documents
1-(2,4,6-Triisopropylphenyl)ethylamine: A new chiral auxiliary for the asymmetric synthesis of γ-amino acid derivatives
Cividino, Pascale,Py, Sandrine,Delair, Philippe,Greene, Andrew E.
, p. 485 - 493 (2007/10/03)
The title compound has proven to be an excellent chiral auxiliary for nitrones in SmI2-mediated reductive coupling with α,β-unsaturated esters. A variety of such nitrones, prepared from aldehydes and enantiopure N-hydroxy-1-(2,4,6-triisopropylp
