77921-36-9 Usage
Uses
Used in Pharmaceutical Industry:
Venlafaxine is used as an antidepressant and anxiolytic medication for the treatment of major depressive disorder, generalized anxiety disorder, social anxiety disorder, and panic disorder. It is effective in modulating the levels of serotonin and norepinephrine in the brain, which are essential for maintaining a healthy mood and emotional balance.
Used in Clinical Psychiatry:
In the field of clinical psychiatry, venlafaxine is utilized as a therapeutic agent to manage various mental health conditions. Its ability to increase the levels of serotonin and norepinephrine in the brain makes it a valuable tool in the treatment of depression and anxiety disorders.
Used in Research and Development:
Venlafaxine is also used in research and development for the study of the underlying mechanisms of depression and anxiety, as well as the development of new medications with similar or improved therapeutic effects. Understanding the action of venlafaxine can provide insights into the development of novel treatments for mood disorders.
Common side effects of venlafaxine include nausea, dizziness, dry mouth, and insomnia. It is available in both immediate-release and extended-release formulations and is typically taken orally. It is crucial to follow the prescribed dosage and consult with a healthcare professional before using venlafaxine to ensure its safe and effective use.
Check Digit Verification of cas no
The CAS Registry Mumber 77921-36-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,9,2 and 1 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 77921-36:
(7*7)+(6*7)+(5*9)+(4*2)+(3*1)+(2*3)+(1*6)=159
159 % 10 = 9
So 77921-36-9 is a valid CAS Registry Number.
77921-36-9Relevant academic research and scientific papers
The reaction of some nuclear substituted acyclic conjugated styryl ketones and related Mannich bases with ethanethiol.
Dimmock, J.R.,Smith, L.M.,Smith, P.J.
, p. 984 - 991 (2007/10/02)
The second order rate constants for the reaction of ethanethiol with a number of conjugated nuclear-substituted styryl ketones and related Mannich bases in 50percent aqueous acetonitrile was undertaken.Variation of the alkyl group adjacent to the carbonyl
