Woods, Thomas S. published the artcileCleavage of sulfur-sulfur bonds with sodium hydrogen selenide, Computed Properties of 14807-75-1, the publication is Journal of Organic Chemistry (1974), 39(25), 3716-20, database is CAplus.
Sodium hydrogen selenide is shown to be an effective reagent for reduction of alkyl, aryl, aralkyl, and functionally substituted disulfides to thiols under mild conditions in protic solvents. Two-electron transfer from the hydrogen selenide anion, which promotes the cleavage of the S-S bond with concomitant production of elemental selenium, is found to occur only in a narrow pH range. Organic thiosulfates (Bunte salts) also give thiols through the intermediacy of the corresponding disulfide on reaction with sodium hydrogen selenide.
Journal of Organic Chemistry published new progress about 14807-75-1. 14807-75-1 belongs to ethers-buliding-blocks, auxiliary class Salt,Thiourea,Amine,Aliphatic hydrocarbon chain, name is Formamidine disulfide dihydrochloride, and the molecular formula is C4H6BrN3, Computed Properties of 14807-75-1.
Referemce:
https://en.wikipedia.org/wiki/Ether,
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