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1357363-89-3

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1357363-89-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1357363-89-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,5,7,3,6 and 3 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1357363-89:
(9*1)+(8*3)+(7*5)+(6*7)+(5*3)+(4*6)+(3*3)+(2*8)+(1*9)=183
183 % 10 = 3
So 1357363-89-3 is a valid CAS Registry Number.

1357363-89-3Downstream Products

1357363-89-3Relevant articles and documents

Thiol, disulfide, and trisulfide complexes of Ru porphyrins: Potential models for iron-sulfur bonds in heme proteins

Reboucas, Julio S.,Patrick, Brian O.,James, Brian R.

, p. 3555 - 3570 (2012/04/10)

Thirty-two Ru(porp)L2 complexes have been synthesized, where porp = the dianion of meso-tetramesitylporphyrin (TMP) or meso-tetrakis(4- methylphenyl)porphyrin (H2T-pMe-PP), and L = a thiol, a sulfide, a disulfide, or a trisulfide. Species studied were with RSH [R = Me, Et, nPr, iPr, tBu, Bn (benzyl), and Ph], RSR (R = Me, Bn), RSSR (R = Me, Et, nPr, Bn) and MeSStBu, and RSSSR (R = Me, Bn). All the species except two, which were the isolated Ru(T-pMe-PP)(tBuSH)2 and Ru(TMP)(MeSSMe)2, were characterized in situ. The disulfide complex was characterized by X-ray analysis. 1H NMR data for the coordinated thiols are the first reported within metalloporphyrin systems, and are especially informative because of the upfield shifts of the axial sulfur-containing ligands due to the porphyrin π-ring current effect, which is also present in the di- and trisulfide species. The disulfide in the solid state structure of Ru(TMP)(MeSSMe)2 is η1(end-on) coordinated, the first example of such bonding in a nontethered, acyclic dialkyl disulfide; 1H-1H EXSY NMR data in solution show that the species undergoes 1,2-S-metallotropic shifts. Stepwise formation of the bis(disulfide) complex from Ru(TMP)(MeCN)2 in solution occurs with a cooperativity effect, resembling behavior of FeII-porphyrin systems where crystal field effects dominate, but ligand trans-effects are more likely in the Ru system. The η1(end-on) coordination mode is also favored for the trisulfide ligand. Discussed also are the remarkable linear correlations that exist between the ring-current shielding shifts for the axial ligand C 1 protons of Ru(porp)(RSxR)2 and x (the number of S atoms). The Introduction briefly reviews literature on Ru- and Fe porphyrins (including heme proteins) with sulfur-containing ligands or substrates, and relationships between our findings and this literature are discussed throughout the paper.

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