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5,5-dimethylthiazolidine-2,4-dicarboxylic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

142185-31-7

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142185-31-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 142185-31-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,2,1,8 and 5 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 142185-31:
(8*1)+(7*4)+(6*2)+(5*1)+(4*8)+(3*5)+(2*3)+(1*1)=107
107 % 10 = 7
So 142185-31-7 is a valid CAS Registry Number.
InChI:InChI=1/C7H11NO4S/c1-7(2)3(5(9)10)8-4(13-7)6(11)12/h3-4,8H,1-2H3,(H,9,10)(H,11,12)/t3-,4-/m1/s1

142185-31-7Downstream Products

142185-31-7Relevant academic research and scientific papers

Removal of toxic tellurium (IV) compounds via bioreduction using flucloxacillin in aqueous acidic medium: A kinetic and mechanistic approach

Fawzy, Ahmed

, (2019/09/06)

This paper describes a novel method for the removal of potassium tellurite (TeIV), a toxic tellurium (IV) compound, via its bioreduction using the drug flucloxacillin (Flx) in an aqueous sulfuric acid solution. The kinetics of the bioreduction process were monitored using UV–Vis absorption spectra at an ionic strength of 2.0 mol dm?3 and 298 K. The reaction between TeIV and Flx was set at a 1:1 stoichiometry. The reduction reaction followed first-order kinetics for [Flx] and fractional-first-order kinetics for [TeIV] and [H+]. The effects of ionic strength and relative permittivity of the reaction medium were also explored. Supplementation with divalent transition metal ions enhanced the reduction rate. The reaction products were identified, in order of their stoichiometric results, spot tests and FT-IR spectra as 3-(2-chloro-6-fluorophenyl)-5-methylisoxazol-4-carbocylic acid, 5,5-dimethyl-thiazolidine-2,4-dicarboxlic acid, ammonium ion, carbon dioxide and elemental tellurium (Te0). The reaction rate dependence on temperature was studied, and the activation and thermodynamic parameters were assessed and discussed. The derived rate-law expression was found to be in excellent accordance with the acquired investigational outcomes. A conceivable reaction mechanism has been provided, which includes a reaction between the protonated flucloxacillin (Flx+) and tellurous acid (H2TeO3) as the essential reactive species, resulting in the construction of an intermediate complex. Such complex decays in the rate-determining step to yield the final reaction products.

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