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214550-11-5

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214550-11-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 214550-11-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,4,5,5 and 0 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 214550-11:
(8*2)+(7*1)+(6*4)+(5*5)+(4*5)+(3*0)+(2*1)+(1*1)=95
95 % 10 = 5
So 214550-11-5 is a valid CAS Registry Number.

214550-11-5Downstream Products

214550-11-5Relevant articles and documents

Use of Intraligand CH Coupling Constants to Assess Binding in Organometallic Compounds. Insight into Electronic and Steric Properties of Monodentate P-Donor Ligands

Moore, Scott J.,Marzilli, Luigi G.

, p. 5329 - 5335 (2008/10/08)

In a series of methyleobaloximes (LCo(DH)2CH3, where DH = monoanion of dimethylglyoxime), the influence of P-donor ligands (L) on 1JCH values of the Co-CH3 moiety correlated well with the pKa of L except when L was bulky (Cy3P and i-Pr3P). In contrast, no single steric parameter of those known for the trivalent P donors examined could be used to describe the variance of 1JCH. The results indicate that the dominant property of L influencing this: 1JCH is electron donation. Although poor, the best correlation with a steric parameter was found with calculated cone angles (CCA) determined by experimental methods on methanol-coordinated cobaloximes. Since the single parameter fits with pKa indicated a steric effect, multiparameter regressions were performed using various combinations of electronic and steric terms. Terms reflecting only σ-donor ability (e.g., pKa) gave better correlations than terms reflecting combinations of σ-donor and π-acceptor properties (e.g., Σχ). CCA values also resulted in better multiparameter fits of the data than other reported steric terms. Using a multiparameter approach also allowed for the simultaneous fit of data for L = phosphine and phosphite ligands. Correlations of this type were poor with single parameter fits. The sensitivity of 1JCH to trans ligand electronic and steric effects indicates that small changes in the hybridization of the Co-CH3 moiety occur. This method allows us to probe the nature of Co-C bonding in the ground slate. The other experimental methods for probing this bond (e.g., X-ray crystallography, FT-Raman spectroscopy, etc.) indicate that this bond is relatively insensitive to the trans ligand in the ground state. Thus, 1JCH values may be a useful general method for examining B12 systems and also hold promise for other types of organometallic compounds.

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