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N2C3H2(CH2N(C6H11)CH2C5H4N)2 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1295578-63-0

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1295578-63-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1295578-63-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,9,5,5,7 and 8 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1295578-63:
(9*1)+(8*2)+(7*9)+(6*5)+(5*5)+(4*7)+(3*8)+(2*6)+(1*3)=210
210 % 10 = 0
So 1295578-63-0 is a valid CAS Registry Number.

1295578-63-0Relevant academic research and scientific papers

From pyrazolate-based binuclear copper(I) complexes to octanuclear θ-mesityl-bridged μ4-oxo-cuprocuprates: Controlled dioxygen splitting by organocopper scaffolds

Stollenz, Michael,Gehring, Henrike,Konstanzer, Vera,Fischer, Stefan,Dechert, Sebastian,Grosse, Christian,Meyer, Franc

, p. 3708 - 3725 (2011/09/20)

The synthesis of a series of new pyrazole-based binucleating compartmental ligands, 3,5-bis(R2R3N)-(4-R1)-pyrazoles L 1H-L6H (L1H, R1 = H, R2 = Me, R3 = 2-py(CH2); L2H, R1 = Ph, R2 = Me, R3 = 2-py(CH2); L3H, R 1 = H, R2 = Cy, R3 = 2-py(CH2); L4H, R1 = Ph, R2 = Cy, R3 = 2-py(CH2); L5H, R1 = Ph, R2, R 3 = 2-py(CH2), L6H, R1 = Ph, R 2 = Me, R3 = 8-quin), together with the X-ray crystal structure of L3H is reported. After deprotonation and subsequent reaction with 2 equiv of [CuI(CH3CN)4](BF 4) and PMe3, L3H forms the stable binuclear CuI complex [L3{Cu(PMe3)}2](BF 4) (1). The analogous reaction with L6H and 2 equiv of tert-butyl isonitrile affords [L6{Cu(CNtBu)}2](BF 4) (2). 1 and 2 represent the first examples of binuclear Cu I-pyrazolate complexes of the type [LCuI2]X that have been characterized by their X-ray crystal structures. With respect to the planes spanned by the pyrazolate backbone, 1 shows a cis orientation of the PMe3 ligands, whereas 2 exhibits a trans arrangement of the tBuNC ligands. L1H-L6H are shown to react with 4 equiv of mesitylcopper and stoichiometric amounts of dioxygen, leading to the formation of the unusually stable organocopper frameworks 3-8. These complexes follow a general structural principle that is best described by the heteroleptic O-centered cuprate anion [(MesCuI)4(μ4-O)] 2- linked via four trans-oriented θ-mesityl bridges to two flanking binuclear CuI-pyrazolates [(L1-L 6)CuI2]+. Thus, 1 and 2 can also be viewed as capping binuclear CuI-complex units that are concealed by two ancillary PMe3 and tBuNC ligands, respectively. The exemplary reaction of 4 with an excess of dimethyl acetylenedicarboxylate (DMDAC) supports the observed cuprate features of 3-8, since after hydrolysis the corresponding (syn-)addition product MesC(CO2Me)=C(CO2Me)H (9) and the free ligand L2H are found as major products.

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