88738-57-2 Usage
General Description
The chemical 2-(benzylsulfinyl)-N,N-diethylethanamine, also known as modafinil, is a medication that is used to promote wakefulness in individuals with conditions such as narcolepsy, obstructive sleep apnea, and shift work sleep disorder. It works by affecting certain neurotransmitters in the brain, leading to increased alertness and reduced feelings of fatigue. Modafinil is a central nervous system stimulant and is classified as a schedule IV controlled substance due to its potential for abuse and addiction. It is typically taken orally and has a relatively long duration of action, making it effective for promoting wakefulness throughout the day. Despite potential side effects such as headache, nausea, and dizziness, modafinil is considered a valuable treatment option for individuals struggling with excessive daytime sleepiness.
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 articles and documents
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.
