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620605-53-0

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620605-53-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 620605-53-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,2,0,6,0 and 5 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 620605-53:
(8*6)+(7*2)+(6*0)+(5*6)+(4*0)+(3*5)+(2*5)+(1*3)=120
120 % 10 = 0
So 620605-53-0 is a valid CAS Registry Number.

620605-53-0Downstream Products

620605-53-0Relevant academic research and scientific papers

Frustrated Lewis pairs: Reactivities of TMS protected amines and phosphines in the presence of B(C6F5)3

Schulz, Felix,Sumerin, Victor,Leskelae, Markku,Repo, Timo,Rieger, Bernhard

supporting information; experimental part, p. 1920 - 1922 (2010/05/15)

TMS protected amines in combination with B(C6F5) 3 were found to activate H2 and this is followed by a cleavage of the N-Si bond and the generation of TMSH. A TMS protected phosphine on the other hand reacts rap

Experimental and theoretical investigations of tellurium(IV) diimides and imidotelluroxanes: X-ray structures of B(C6F5)3 adducts of OTe(μ-NtBu)2TeNtBu, [OTe(μ-NtBu)2Te(μ-O)]2 and tBuNH2

Schatte, Gabriele,Chivers, Tristram,Tuononen, Heikki M.,Suontamo, Reijo,Laitinen, Risto,Valkonen, Jussi

, p. 443 - 451 (2008/10/09)

The hydrolysis of tBuNTe(μ-NtBu) 2TeNtBu (1) with 1 or 2 equiv of (C6F 5)3B·H2O results in the successive replacement of terminal imido groups by oxo ligands to give the telluroxane-Lewis acid adducts (C6F5)3B· OTe(μ-NtBu)2TeNtBu (2) and [(C 6F5)3B·OTe(μ-NtBu) 2Te(μ-O)]2 (3), which were characterized by multinuclear NMR spectroscopy and X-ray crystallography. The Te=O distance in 2 is 1.870(2) A?. The di-adduct 3 involves the association of four BuNTeO monomers to give a tetramer in which both terminal Te=O groups [d(TeO) = 1.866(3) A?] are coordinated to B(C6F5)3. The central Te2O2 ring in 3 is distinctly unsymmetrical [d(TeO) = 1.912(3) and 2.088(2) A?]. The X-ray structure of (C 6F5)3B·NH2tBu (4), the byproduct of these hydrolysis reactions, is also reported. The geometries and energies of tellurium(IV) diimides and imido telluroxanes were determined using quantum chemical calculations. The calculated energies for the reactions E(NR)2 + Te(NR)2 (E = S, Se, Te; R = H, Me, Bu, SiMe 3) confirm that cyclodimerization of tellurium(IV) diimides is strongly exothermic. In the mixed-chalcogen systems, the cycloaddition is energetically favorable for the Se/Te combination. The calculated energies for the further oligomerization of the dimers XE(μ-NMe)2EX (E = Se, Te; X = NMe, O) indicate that the formation of tetramers is strongly exothermic for the tellurium systems but endothermic (X = NMe) or thermoneutral (X = O) for the selenium systems, consistent with experimental observations.

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