The three-dimensional configuration of the ester heterocycle is basically the same as that of the carbocycle. Compound: 4,4-Dipyridyl Disulfide(SMILESS: C1(SSC2=CC=NC=C2)=CC=NC=C1,cas:2645-22-9) is researched.Computed Properties of C6H12N2O4Pt. The article 《Iron-Catalyzed Thiolation and Selenylation of Cycloalkyl Hydroperoxides via C-C Bond Cleavage》 in relation to this compound, is published in Journal of Organic Chemistry. Let’s take a look at the latest research on this compound (cas:2645-22-9).
A cheap iron-catalyzed C-C bond cleavage and thiolation/selenylation of cycloalkyl hydroperoxides I [R = Ph, 2-thienyl, 2-naphthyl, etc.; R1 = H, Me, n-heptyl; X = (CH2)n; n = 1-4, 8] are presented. This redox-neutral protocol provides efficient access to diverse distal keto-functionalized thioethers and selenium compounds II (R = n-pentyl, Ph, 2-thienyl, etc.; R1 = H, Me, n-heptyl; Ar = Ph, 4-MeC6H4, 2-pyridyl, etc.; X = (CH2)n; n = 1-4, 8; Y = S, Se). Remarkably, only some amounts of disulfides are required for this transformation.
After consulting a lot of data, we found that this compound(2645-22-9)Application In Synthesis of 4,4-Dipyridyl Disulfide can be used in many types of reactions. And in most cases, this compound has more advantages.
Reference:
Bromide – Wikipedia,
bromide – Wiktionary