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The chemical compound "(C4H2N)3(C4H2N(CC(C6(2)H4Cl)2))(C(C6H5))4FeN3" is a complex organic molecule with a central iron atom. It features three (C4H2N) groups, which are likely to be pyridine-like structures, and one (C4H2N(CC(C6(2)H4Cl)2)) group, which suggests the presence of a pyridine ring with attached chlorinated phenyl groups. The compound also includes four phenyl groups (C(C6H5)), which are benzene rings, and a tridentate nitrogen ligand (N3). This molecule is likely to be a coordination complex with iron, where the iron atom is coordinated to the nitrogen atoms from the pyridine and phenyl groups, forming a stable complex. The presence of chlorine atoms in the phenyl rings indicates that the compound may have potential applications in areas where halogenated aromatic compounds are used, such as in pharmaceuticals or materials science.

97170-33-7

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97170-33-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 97170-33-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,7,1,7 and 0 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 97170-33:
(7*9)+(6*7)+(5*1)+(4*7)+(3*0)+(2*3)+(1*3)=147
147 % 10 = 7
So 97170-33-7 is a valid CAS Registry Number.

97170-33-7Downstream Products

97170-33-7Relevant academic research and scientific papers

Proton nuclear magnetic resonance studies of iron porphyrin complexes with a vinyl carbene inserted between iron and a pyrrole nitrogen

Balch, Alan L.,Cheng, Ru-Jen,La Mar, Gerd N.,Latos-Grazynski, Lechoslaw

, p. 2651 - 2656 (2008/10/08)

Proton NMR spectra have been obtained for the paramagnetic (S = 3/2) iron(III) complexes P[C=C(p-C6H4Cl)2]FeX (X = Cl, Br, I; P = porphyrin dianion from meso-tetraarylporphyrin, or protoporphyrin IX dimethyl ester). Functional group assignments have been made with use of selective deuterium and methyl labeling. More detailed assignments have been made on the basis of the temperature dependence of the spectra and analysis of the line widths, which are dominated by dipolar relaxation. The spectra are indicative of Cs symmetry for these complexes in solution. This result is in accord with the solid-state structure of these complexes but requires some oscillatory motion of one of the P-ClC6H4 groups. The dominant π-spin transfer to the pyrroles indicates that, of the alternate ground states (dxy)2(dxz)1(dyz) 1(dx2-y2)1 and (dxy)2(dxz)1(dyz) 1(dz2)1, the latter is present. The complexes exhibit axial magnetic anisotropy dominated by negative zero-field splitting. For the protoporphyrin IX derivative, the spectrum indicates that the four isomers resulting from carbene insertion into each of the four distinct Fe-N bonds are present.

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