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η(5)-CpCo(C3F7)(dimethylphenylphosphine)(I) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

186315-72-0

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186315-72-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 186315-72-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,6,3,1 and 5 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 186315-72:
(8*1)+(7*8)+(6*6)+(5*3)+(4*1)+(3*5)+(2*7)+(1*2)=150
150 % 10 = 0
So 186315-72-0 is a valid CAS Registry Number.

186315-72-0Upstream product

186315-72-0Downstream Products

186315-72-0Relevant academic research and scientific papers

Evidence for an intramolecular transition metal Arbusov reaction

Chen, Zhao,Jablonski, Chet,Bridson, John

, p. 2083 - 2094 (1996)

Reaction of [CpCo(C3F7)(I)(L)], (L = PPh2Me (1a), PPhMe2 (1b), PMe3 (1c), and PPh(OMe)2 (2)), with PPh(OMe)2 affords diastereomeric Co- and P-chiral metallophosphinates CpCo(C3F7)(L)(P(O)Ph(OMe)), 4a,b,c and 6, respectively. The solid state structure and relative configuration of the lower Rf diastereomeric phosphinate CpCo(C3F7)(PPh(OMe)2)(P(O)Ph(OMe)), 6-2, was determined by X-ray diffraction. RR;SS-6-2 crystallizes in the triclinic system with space group P1(no. 2), with a = 12.928(4) A, b = 14.683(4) A, c = 7.666(2) A, α = 103.50(2)°, β = 101.31(3)°, γ = 109.50(2)°, V = 1272.8(7) A3, Z = 2, and R = 0.036 (Rw = 0.030) for 2867 reflections with I > 3.00σ(I). CpCo(C3F7)(I)(PPh(OMe)2), 2, reacts with PPh2Me to yield the same Co- and P-chiral phosphinate products as obtained for the reaction of 1a with PPh(OMe)2, albeit with different optical yields. The product stereochemistry is not accounted for by the established mechanism for transition metal Arbuzov-like dealkylations, which requires formation of a common, ionic intermediate [CpCo(C3F7)(PPh2Me)(PPh(OMe)2)] +, 3, via iodide substitution and subsequent nucleophilic attack at carbon. A parallel intramolecular dealkylation pathway is proposed to account for the results.

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