Tanifuji, Kazuki published the artcileA Convenient Route to Synthetic Analogues of the Oxidized Form of High-Potential Iron-Sulfur Proteins, Product Details of C15H24S, the publication is Inorganic Chemistry (2014), 53(8), 4000-4009, database is CAplus and MEDLINE.
An amide-bound [Fe4S4]3+ cluster, [Fe4S4{N(SiMe3)2}4]– (1), was found to serve as a convenient precursor for synthetic analogs of the oxidized form of high-potential Fe-S proteins. Treatment of 1 with 4 equiv of bulky thiols led to replacement of the amide ligands with thiolates, giving rise to [Fe4S4(SR)4]– clusters (R = Dmp (2a), Tbt (2b), Eind (2c), Dxp (2d), Dpp (2e); Dmp = 2,6-di(mesityl)phenyl, Tbt = 2,4,6-tris[bis(trimethylsilyl)methyl]phenyl, Eind = 1,1,3,3,5,5,7,7-octaethyl-s-hydrindacen-4-yl, Dxp = 2,6-di(m-xylyl)phenyl, Dpp = 2,6-diphenylphenyl). These clusters were characterized by the mass spectrum, the EPR spectrum, and x-ray crystallog. The redox potentials of the [Fe4S4]3+/2+ couple, -0.82 V (2a), -0.86 V (2b), -0.84 V (2c), -0.74 V (2d), and -0.63 V (2e) vs. Ag/Ag+ in THF, are significantly more neg. than that of [Fe4S4(SPh)4]-/2- (-0.21 V).
Inorganic Chemistry published new progress about 22693-41-0. 22693-41-0 belongs to catalysis-chemistry, auxiliary class Other Functionalization Reagent, name is 2,4,6-Triisopropylbenzenethiol, and the molecular formula is C5H6N2O2, Product Details of C15H24S.
Referemce:
https://courses.lumenlearning.com/boundless-chemistry/chapter/catalysis/,
Catalysis – Wikipedia