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22286-99-3

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22286-99-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 22286-99-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,2,8 and 6 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 22286-99:
(7*2)+(6*2)+(5*2)+(4*8)+(3*6)+(2*9)+(1*9)=113
113 % 10 = 3
So 22286-99-3 is a valid CAS Registry Number.

22286-99-3Relevant articles and documents

Crystal Structure and Catalytic Behavior in Olefin Epoxidation of a One-Dimensional Tungsten Oxide/Bipyridine Hybrid

Amarante, Tatiana R.,Antunes, Margarida M.,Valente, Anabela A.,Paz, Filipe A. Almeida,Pillinger, Martyn,Gon?alves, Isabel S.

, p. 9690 - 9703 (2015/11/03)

The tungsten oxide/2,2′-bipyridine hybrid material [WO3(2,2′-bpy)]·nH2O (n = 1-2) (1) has been prepared in near quantitative yield by the reaction of H2WO4, 2,2′-bpy, and H2O in the mole ratio of ca. 1:2:700 at 160°C for 98 h in a rotating Teflon-lined digestion bomb. The solid-state structure of 1 was solved and refined through Rietveld analysis of high-resolution synchrotron X-ray diffraction data collected for the microcrystalline powder. The material, crystallizing in the orthorhombic space group Iba2, is composed of a one-dimensional organic-inorganic hybrid polymer, ∞1[WO3(2,2′-bpy)], topologically identical to that found in the previously reported anhydrous phases [MO3(2,2′-bpy)] (M = Mo, W). While in the latter the N,N′-chelated 2,2′-bpy ligands of adjacent corner-shared {MO4N2} octahedra are positioned on the same side of the 1D chain, in 1 the 2,2′-bpy ligands alternate above and below the chain. The catalytic behavior of compound 1 for the epoxidation of cis-cyclooctene was compared with that for several other tungsten- or molybdenum-based (pre)catalysts, including the hybrid polymer [MoO3(2,2′-bpy)]. While the latter exhibits superior performance when tert-butyl hydroperoxide (TBHP) is used as the oxidant, compound 1 is superior when aqueous hydrogen peroxide is used, allowing near-quantitative conversion of the olefin to the epoxide. With H2O2, compounds 1 and [MoO3(2,2′-bpy)] act as sources of soluble active species, namely, the oxodiperoxo complex [MO(O2)2(2,2′-bpy)], which is formed in situ. Compounds 1 and [WO(O2)2(2,2′-bpy)] (2) were further tested in the epoxidation of cyclododecene, trans-2-octene, 1-octene, (R)-limonene, and styrene. The structure of 2 was determined by single-crystal X-ray diffraction and found to be isotypical with the molybdenum analogue.

Highly active manganese-containing polyoxometalate as catalyst for epoxidation of alkenes with hydrogen peroxide

Neumann, Ronny,Gara, Mohammad

, p. 5509 - 5510 (2007/10/02)

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Condensation of Propiolactones with Phosphorus Ylides: a Convenient Synthesis of α,β-Ethylenic Ketones

Le Roux, Juliette,Le Corre, Maurice

, p. 1464 - 1465 (2007/10/02)

δ-Hydroxy-β-ketophosphoranes have been obtained by condensation of propiolactones with ylides and afforded α,β-unsaturated ketones on heating.

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