Saleh, Azhari published the artcileThe acid-catalyzed hydrolysis of episulfoxides, Safety of 1,2-Bis(2-chloroethyl)disulfane, the publication is Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999) (1981), 132-9, database is CAplus.
The acid-catalyzed hydrolyses of the episulfoxides I (R = H, Me, Ph, CHMe2, CMe3, Et) in aqueous mineral acids were studied kinetically. I (R = H, Me, Ph) was hydrolyzed by concurrent A-2 and nucleophile-catalyzed pathways. Hydrolysis of I (R = CHMe2, CMe3) in H2SO4 occurred by an A-2 mechanism, but in concentrated HClO4 their rate profiles passed through a maximum with a changeover from an A-2 to an A-1 mechanism. The protonation behavior of these 2 episulfoxides was studied, pKBH+ values being determined
Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999) published new progress about 1002-41-1. 1002-41-1 belongs to chlorides-buliding-blocks, auxiliary class Aliphatic Chain, name is 1,2-Bis(2-chloroethyl)disulfane, and the molecular formula is C4H8Cl2S2, Safety of 1,2-Bis(2-chloroethyl)disulfane.
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https://en.wikipedia.org/wiki/Chloride,
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