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(CH3O)2C6H2N2C20H6(C6H5)4N4Zn is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

286386-50-3

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286386-50-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 286386-50-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,8,6,3,8 and 6 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 286386-50:
(8*2)+(7*8)+(6*6)+(5*3)+(4*8)+(3*6)+(2*5)+(1*0)=183
183 % 10 = 3
So 286386-50-3 is a valid CAS Registry Number.

286386-50-3Relevant academic research and scientific papers

Cavitand-porphyrins

Starnes,Rudkevich,Rebek, Jr.

, p. 4659 - 4669 (2007/10/03)

The synthesis and characterization of new nanoscale container molecules 7 and 8 are described. They are covalent hybrids of deepened, self-folding cavitands and metalloporphyrins. In receptor 7, the Zn-porphyrin wall is directly built onto the cavitand skeleton. Host 8 features a large unimolecular cavity containing two cavitands attached with the Zn-porphyrin wall. Its dimensions, ~10 × 25 A, place it among the largest synthetic hosts prepared to date. A series of adamantyl- and pyridyl-containing guests 14-20 of various lengths were prepared and used to determine the hosts' binding abilities in solution using UV/vis and 1H NMR spectroscopy. Intramolecular hydrogen bonds at the upper rims of the cavitands resist the unfolding of the inner cavities and thereby increase the energetic barrier to guest exchange. The exchange is slow on the NMR time scale (at ≤300 K), and kinetically stable complexes result. When the cavities and metalloporphyrins participate simultaneously in the binding event, very high affinities for guests are found (-ΔG295 up to 10 kcal mol-1 in toluene), to which the porphyrin fragments contribute significantly (-ΔG295 up to 6 kcal mol-1). The pairwise selection of two different guests by molecular container 8 is reported, and the termolecular complex formed raises the possibility of metal-catalyzed bimolecular reactions in these containers.

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