88738-57-2 Usage
Uses
Used in Pharmaceutical Industry:
2-(Benzylsulfinyl)-N,N-diethylethanamine is used as a wakefulness-promoting agent for the treatment of excessive daytime sleepiness associated with narcolepsy, obstructive sleep apnea, and shift work sleep disorder. It functions by affecting neurotransmitters in the brain, leading to increased alertness and reduced feelings of fatigue, making it a valuable treatment option for individuals struggling with these conditions.
Used in Neurology:
In the field of neurology, 2-(benzylsulfinyl)-N,N-diethylethanamine is utilized as a medication to address sleep disorders characterized by excessive sleepiness during the day. Its ability to stimulate the central nervous system and modulate neurotransmitters makes it an effective treatment for patients with narcolepsy, obstructive sleep apnea, and those experiencing sleep disturbances due to shift work.
Used in Sleep Medicine:
2-(Benzylsulfinyl)-N,N-diethylethanamine is employed as a therapeutic agent in sleep medicine to manage sleep disorders that result in excessive daytime sleepiness. Its long duration of action and oral administration make it a convenient and effective option for patients seeking relief from the impact of their sleep disorders on daily functioning and quality of life.
Check Digit Verification of cas no
The CAS Registry Mumber 88738-57-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,7,3 and 8 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 88738-57:
(7*8)+(6*8)+(5*7)+(4*3)+(3*8)+(2*5)+(1*7)=192
192 % 10 = 2
So 88738-57-2 is a valid CAS Registry Number.
88738-57-2Relevant academic research and scientific papers
GOLD(III) CATALYZED OXIDATION OF SULFIDES TO SULFOXIDES BY NITRIC ACID UNDER PHASE-TRANSFER CONDITIONS: A NEW SYNTHESIS OF SULFOXIDES
Gasparrini, F.,Giovannoli, M.,Misiti, D.,Natile, G.,Palmieri, G.
, p. 3181 - 3184 (2007/10/02)
Gold(III) halides catalyze the oxidation of sulfides to sulfoxides in a phase-transfer process.The organic sulfides, dissolved in nitromethane, are treated with (Bu4N(1+)*AuCl4(1-)) in catalytic amount and aqueous nitric acid wich acts as an oxidant.The oxidation of the thio-group is selective and can be carried out also in the presence of other oxidizable groups, such as vinyl, tertiary amino, hydroxy, diol etc, which are left unchanged.Moreover in the case of asymmetric disulfides the reaction is regiospecific leading to the fomation of a single monosulfoxide.
