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46132-92-7

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46132-92-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 46132-92-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,6,1,3 and 2 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 46132-92:
(7*4)+(6*6)+(5*1)+(4*3)+(3*2)+(2*9)+(1*2)=107
107 % 10 = 7
So 46132-92-7 is a valid CAS Registry Number.

46132-92-7Downstream Products

46132-92-7Relevant academic research and scientific papers

Unambiguous characterization of p-cresyl sulfate, a protein-bound uremic toxin, as biomarker of heart and kidney disease

Paroni, Rita,Casati, Silvana,Dei Cas, Michele,Bignotto, Monica,Rubino, Federico Maria,Ciuffreda, Pierangela

, (2019)

p-Cresyl sulfate is one of the bound uremic toxins whose level increases in the sera of patients with the severity of chronic kidney disease and is therefore used as a standard for clinical investigations. Our first attempts to obtain p-cresyl sulfate led

Reactivity-Selectivity Correlations. 4. The α Effect in SN2 Reactions at sp3 Carbon. The Reactions of Hydrogen Peroxide Anion with Methyl Phenyl Sufates

Buncel, Erwin,Wilson, Harold,Chuaqui, Claudio

, p. 4896 - 4900 (2007/10/02)

A kinetic study is reported of the reactions of substituted phenyl methyl sulfates with hydrogen peroxide and methoxide ion in methanol solvent at 25 deg C.Dissection of the rate data for the H2O2/MeONa system allows the specific coefficients kHOO- and kMeO- to be evaluated.Hydroperoxide anion is found to be more reactive than methoxide ion (kHOO-/kMeO- varies from 6 to 11 depending on the sustrate), indicating than an α effect is operating for this nucleophilic attack at saturated carbon.This is in agreement with earlier results on the enhanced reactivity of hydrazine relative to glycine ethyl ester.The results further show that the Hammett p value for the α nucleophiles is smaller than for the normal nucleophiles; however an inverse order is found for the respective Bronsted β values.Analysis of these contrasting relationships in terms of reaction coordinate diagrams leads to the conclusion that the ordinary two-dimensional reaction coordinate is not applicable to the α nucleophiles and that significant anti-Hammond effects arise in these cases.The shift in the transition state perpendicular to the diagonal is discussed in terms of destabilization of the α nucleophile or via a tight transition-state structure as previously suggested for transmethylation.It is concluded that the Hammett p value is a valid criterion of the reactivity-selectivity principle (RSP) for the normal nucleophiles which conform to the two-dimensional representation but not for the α nucleophiles.This leads to a limitation on the applicability of the RCP as a measure of transition-state structure.

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