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1445947-53-4

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1445947-53-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1445947-53-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,4,5,9,4 and 7 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1445947-53:
(9*1)+(8*4)+(7*4)+(6*5)+(5*9)+(4*4)+(3*7)+(2*5)+(1*3)=194
194 % 10 = 4
So 1445947-53-4 is a valid CAS Registry Number.

1445947-53-4Downstream Products

1445947-53-4Relevant academic research and scientific papers

From triplesalen to triplesalalen and triplesalan - Strengthening the aromatic character of the ligand backbone in extended phloroglucinol ligands by prevention of heteroradialene formation

Feldscher, Bastian,Stammler, Anja,Boegge, Hartmut,Glaser, Thorsten

, p. 388 - 397 (2013)

The methyl-protected triplesalalen ligand Me3H 3talalen tBu 2 was synthesized from 2,4,6-tris(bromomethyl)-1,3,5- trimethoxybenzene and three equivalents of the secondary amine 4,6-di-tert-butyl-2-{[2-(methylamino)ethylimino]methyl}phenol. A reduction with NaBH4 afforded the methyl-protected triplesalan ligand Me 3H3talan tBu 2. Deprotection efforts of the methyl-protected Me3H3talalen tBu 2 ligand with Lewis acids were unsuccessful. Using CuII ions as Lewis acid resulted in the formation of the methyl-protected triplesalalen complex [(Me 3H3talalen tBu 2){CuII(H2O)} 3](ClO4)3, which could be characterized by single-crystal X-ray diffraction. The bond-length analysis reveals the aromatic character of the central backbone without heteroradialene contribution, and this is corroborated by NMR spectra of the ligands, which exhibit a singlet assigned to the benzylic protons at δ = 3.50 ppm in the 1H NMR and a resonance typical for an aromatic CAr-O group at δ = 160.0 ppm in the 13C NMR spectroscopy. FTIR spectra of the ligands and of the complexes exhibit the typical features of a central aromatic unit and do not show the characteristic intense bands for vibrations of the exocyclic C=C and C=O double bonds of a heteroradialene. Additionally, the characteristic strong absorption bands for heteroradialenes in the 26000-35000 cm-1 region are absent in the UV/Vis/NIR spectra. The electrochemistry exhibits the reversible oxidation of the terminal phenolates of [(Me3H 3talalen tBu 2){CuII(H2O)}3] (ClO4)3 at +0.72 V vs Fc+/Fc, and the magnetic measurements reveal an uncoupled behavior due to the apical coordination of the central methoxy groups to the CuII ions. To synthesize the triplesalalen ligand H6talalen tBu 2, the methyl-protected ligand Me3H3talalen tBu 2 has been prepared from 1. However, methyl deprotection was not successful but resulted in the complex [(Me 3talalen tBu 2){Cu(H2O)}3](ClO 4)3. Copyright

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