88738-54-9 Usage
Molecular structure
Consists of a benzyl group and a sulfinyl group attached to an ethyl acetate molecule.
Usage
Commonly used in organic synthesis, particularly in the production of pharmaceuticals and agrochemicals.
Medical applications
Has shown potential in the treatment of certain types of cancer and as an anti-inflammatory agent.
Chiral reagent
Studied for its use as a chiral reagent in asymmetric synthesis.
Versatility
A versatile compound with a range of potential applications in the field of chemistry and medicine.
Check Digit Verification of cas no
The CAS Registry Mumber 88738-54-9 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 4 respectively.
Calculate Digit Verification of CAS Registry Number 88738-54:
(7*8)+(6*8)+(5*7)+(4*3)+(3*8)+(2*5)+(1*4)=189
189 % 10 = 9
So 88738-54-9 is a valid CAS Registry Number.
88738-54-9Relevant 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.
