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((C4H9)3SiO)3VOP(C4H9)3 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

353300-68-2

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353300-68-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 353300-68-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,5,3,3,0 and 0 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 353300-68:
(8*3)+(7*5)+(6*3)+(5*3)+(4*0)+(3*0)+(2*6)+(1*8)=112
112 % 10 = 2
So 353300-68-2 is a valid CAS Registry Number.

353300-68-2Downstream Products

353300-68-2Relevant academic research and scientific papers

Symmetry and geometry considerations of atom transfer: Deoxygenation of (silox)3WNO and R3PO (R = Me, Ph, tBu) by (silox)3M (M = V, NbL (L = PMe3, 4-picoline), Ta; silox = tBu3SiO)

Veige, Adam S.,Slaughter, LeGrande M.,Lobkovsky, Emil B.,Wolczanski, Peter T.,Matsunaga, Nikita,Decker, Stephen A.,Cundari, Thomas R.

, p. 6204 - 6224 (2003)

Deoxygenations of (silox)3WNO (12) and R3PO (R = Me, Ph, tBu) by M(silox)3 (1-M; M = V, NbL (L = PMe 3, 4-picoline), Ta; silox = tBu3SiO) reflect the consequences of electronic effects enforced by a limiting steric environment. 1-Ta rapidly deoxygenated R3PO (23 °C; R = Me (ΔG°rxn(calcd) = -47 kcal/mol), Ph) but not tBu3PO (85°, >2 days), and cyclometalation competed with deoxygenation of 12 to (silox)3WN (11) and (silox) 3TaO (3-Ta; ΔG°rxn(calcd) = -100 kcal/mol). 1-V deoxygenated 12 slowly and formed stable adducts (silox)3V-OPR 3 (3-OPR3) with OPR3. 1-Nb(4-picoline) (S = 0) and 1-NbPMe3 (S = 1) deoxygenated R3PO (23 °C; R = Me (ΔG° rxn(calcd from 1-Nb) = -47 kcal/mol), Ph) rapidly and 12 slowly (ΔG° rxn(calcd) = -100 kcal/mol), and failed to deoxygenate tBu3PO. Access to a triplet state is critical for substrate (EO) binding, and the S → T barrier of ~17 kcal/mol (calcd) hinders deoxygenations by 1-Ta, while 1-V (S = 1) and 1-Nb (S → T barrier ~2 kcal/mol) are competent. Once binding occurs, significant mixing with an 1A1 excited state derived from population of a σ*-orbital is needed to ensure a low-energy intersystem crossing of the 3A2 (reactant) and 1A1 (product) states. Correlation of a reactant σ*-orbital with a product σ-orbital is required, and the greater the degree of bending in the (silox)3M-O-E angle, the more mixing energetically lowers the intersystem crossing point. The inability of substrates EO = 12 and tBu3PO to attain a bent ∠M-O-E due to sterics explains their slow or negligible deoxygenations. Syntheses of relevant compounds and ramifications of the results are discussed. X-ray structural details are provided for 3-OPMe3 (∠V-O-P = 157.61(9)°), 3-OPtBu3 (∠V-O-P = 180°), 1-NbPMe3, and (silox)3CIWO (9).

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