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623125-40-6

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623125-40-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 623125-40-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,2,3,1,2 and 5 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 623125-40:
(8*6)+(7*2)+(6*3)+(5*1)+(4*2)+(3*5)+(2*4)+(1*0)=116
116 % 10 = 6
So 623125-40-6 is a valid CAS Registry Number.

623125-40-6Downstream Products

623125-40-6Relevant articles and documents

Synthesis of tripod ligands containing mixed donor sets with phosphane and pyrazole donors - Bidentate chelate binding modes and dynamic behaviour of tripod ligands in d8-metal complexes (NiII, PdII, PtII)

Faissner, Ralf,Huttner, Gottfried,Kaifer, Elisabeth,Kircher, Peter,Rutsch, Peter,Zsolnai, Laszlo

, p. 2219 - 2238 (2007/10/03)

The synthesis of a series of tripod ligands MeOCH2C(CH2X)(CH2Y)(CH2Z) (X = PR2; Y, Z = PR′2 or pz; pz = 1-pyrazolyl) based on the 3,3-difunctionalized oxetane Oa[CH2]2Ca(CH2OMs) (CH2Br)(Oa-Ca) as the starting material is described. With their mixed donor sets these ligands coordinate to d8-metal ions in a bidentate binding mode. One of the three donors remains uncoordinated in each case. Coordination of phosphane donors is generally preferred over coordination of pyrazole donors. With bulky phosphanes such as -CH2PMes2, however, pyrazole may compete with PR2, depending on the kind of the d8 fragment. Dynamic exchange between coordinated and noncoordinated pyrazole donors is observed. Tetracoordinate complexes of the general type L2MR2 are formed (L2 symbolizes the tripod ligand in its bidentate chelate binding mode with two donors functions coordinating and the third one serving as a dangling arm; M = NiII, PdII, PtII). With nickel(II) as the d8 species, tetrahedral or square-planar coordination geometries ensue, depending on the kind of donor functions and on the kind of co-ligands R. With palladium(II) and platinum(II) as the d8 centres, square-planar coordination is observed throughout. The size of the chelate cycles varies from six to eight depending on the number of pyrazole entities within the cycle. The conformations and the conformational flexibility characterizing the chelate cycles have been analysed by X-ray analyses and by variable-temperature NMR. The classes of conformations observed may be formally reduced to chair, half-chair and twist-boat conformations. Dynamic exchange between these conformations is observed, In one case, the same compound forms two different types of crystals that differ by the conformation adopted by their chelate cycles, All compounds have been fully characterized by standard analytical techniques including X-ray structure analysis of 14 chelate compounds. ( Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2003).

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