206125-75-9 Usage
Uses
Used in Pharmaceutical Industry:
Fluoxetine is used as an antidepressant for the treatment of depression, anxiety disorders, and obsessive-compulsive disorder. It functions by inhibiting the reuptake of serotonin, thereby increasing its availability in the synaptic cleft and enhancing mood, sleep, and appetite.
Used in Pediatric Medicine:
Fluoxetine is also prescribed for pediatric patients, making it an essential medication in the field of child and adolescent psychiatry. It helps in managing mood disorders and anxiety in younger populations, under the supervision of a healthcare professional.
Used in Research and Development:
Due to its mechanism of action and widespread use, Fluoxetine is often utilized in research studies to better understand the role of serotonin in various psychiatric conditions and to develop new medications with improved efficacy and fewer side effects.
Check Digit Verification of cas no
The CAS Registry Mumber 206125-75-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,6,1,2 and 5 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 206125-75:
(8*2)+(7*0)+(6*6)+(5*1)+(4*2)+(3*5)+(2*7)+(1*5)=99
99 % 10 = 9
So 206125-75-9 is a valid CAS Registry Number.
InChI:InChI=1/C9H11FO2/c1-7(11)6-12-9-4-2-8(10)3-5-9/h2-5,7,11H,6H2,1H3/t7-/m0/s1
206125-75-9Relevant academic research and scientific papers
Selective Cross-Dehydrogenative C(sp3)-H Arylation with Arenes
Hao, Hong-Yan,Mao, Yang-Jie,Xu, Zhen-Yuan,Lou, Shao-Jie,Xu, Dan-Qian
supporting information, p. 2396 - 2402 (2020/03/13)
Selective C(sp3)-C(sp2) bond construction is of central interest in chemical synthesis. Despite the success of classic cross-coupling reactions, the cross-dehydrogenative coupling between inert C(sp3)-H and C(sp2)-H bonds represents an attractive alternative toward new C(sp3)-C(sp2) bonds. Herein, we establish a selective inter-and intramolecular C(sp3)-H arylation of alcohols with nondirected arenes that thereby provides a general pathway to access a wide range of β-arylated alcohols, including tetrahydronaphthalen-2-ols and benzopyran-3-ols, with high to excellent chemo-and regioselectivity.
