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189881-13-8

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189881-13-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 189881-13-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,9,8,8 and 1 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 189881-13:
(8*1)+(7*8)+(6*9)+(5*8)+(4*8)+(3*1)+(2*1)+(1*3)=198
198 % 10 = 8
So 189881-13-8 is a valid CAS Registry Number.

189881-13-8Upstream product

189881-13-8Relevant articles and documents

Oxidation of Thioether Ligands in Pseudotetrahedral Cyclopentadienylruthenium Complexes: Toward a New Stereoselective Synthesis of Chiral Sulfoxides

Schenk, Wolfdieter A.,Frisch, Jürgen,Dürr, Michael,Burzlaff, Nicolai,Stalke, Dietmar,Fleischer, Roland,Adam, Waldemar,Prechtl, Frank,Smerz, Alexander K.

, p. 2372 - 2378 (2008/10/09)

Ionic ruthenium thioether complexes [Cp(LL′)Ru(SRR′)]PF6 (LL′ = Ph2PCH2PPh2 (1), Ph2PC2H4PPh2 (2),(Ph3P, CO) (3), Me2PC2H4PPh2 (4), (S,S)-Ph2PCHMeCHMePPh2 (5), SRR′ = MeSPh (a), MeS-i-Pr (b), MeSBz (c), i-PrSBz (d), EtSBz (e), MeSCy (f), SC4H8 (g)) were synthesized from the corresponding chloro complexes [Cp-(LL′)RuCl] and thioethers. 5a crystallized in the orthorhombic system, space group P212121 (No. 19), with a = 11.269(3) A°, b = 15.104(2) A?, c = 23.177(4) A?, and Z = 4. 5b crystallized in the monoclinic system, space group P21 (No. 4), with a = 10.539(5) A?, b = 16.216(9) A?, c = 11.011(8) A?, β = 106.04(2)°, and Z = 2. A similar ligand exchange reaction yielded the analogous sulfoxide complexes [Cp(LL′)Ru(S(O)RR′)]PF6 (6-10). 10a crystallized in the orthorhombic system, space group P212121 (No. 19), with a = 14.1664(13) A?, b = 15.792-(2) A?, c = 17.641(2) A?, and Z = 4. 10b-0.93CH2Cl2 crystallized in the orthorhombic system, space group P212121 (No. 19), with a = 12.069(2) A?, b = 17.379(2) A?, c = 19.760(5) A?, and Z = 4. The thioether complexes can also be directly converted to sulfoxide complexes with the strong oxygen transfer reagent dimethyldioxirane (DMD). No crossover products are formed when mixtures of two thioether complexes (e.g., 1a/2c or 1c/2a) are treated with DMD, demonstrating that no Ru-S bond cleavage is involved. Moderate diastereoselectivities are observed for the oxygen transfer to chiral, racemic thioether complexes 3 (8-28%) and 4 (34-60%). Oxidation of the (S,S)-CHIRAPHOS complexes 5, however, is highly stereoselective (de = 46-98%). Treatment of the sulfoxide complexes 10 with sodium iodide removes the chiral, nonracemic sulfoxides from the metal with retention of the configuration at sulfur.

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