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851775-72-9

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851775-72-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 851775-72-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,1,7,7 and 5 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 851775-72:
(8*8)+(7*5)+(6*1)+(5*7)+(4*7)+(3*5)+(2*7)+(1*2)=199
199 % 10 = 9
So 851775-72-9 is a valid CAS Registry Number.

851775-72-9Downstream Products

851775-72-9Relevant academic research and scientific papers

Esterification of R/S-ketoprofen with 2-propanol as reactant and solvent catalyzed by Novozym 435 at selected conditions

Toledo, Maria Victoria,Jose, Carla,Collins, Sebastian E.,Bonetto, Rita D.,Ferreira, Maria Lujan,Briand, Laura E.

, p. 108 - 119 (2012)

The enzymatic esterification of R/S-ketoprofen with 2-propanol catalyzed with the commercial biocatalyst Novozym 435 is addressed in this investigation. The low reaction rate registered in this reaction was investigated in terms of the effect of the alcohol on the physicochemical- enzymatic stability of the biocatalyst and the interaction of the substrates with the catalytic triad at a molecular level. The effect of contacting 2-propanol:H2O mixture on Novozym 435 was investigated at 45 °C for an extended period of time (8 days). The mixture dissolves the polymethylmethacrylate (PMMA) that constitutes the support of the Candida antarctica B lipase (CALB). Additionally, the alcohol diffuses into the biocatalyst's beads remaining strongly adsorbed (the alcohol desorption is evidenced only upon heating at 187 °C) and altering the inner texture of the biocatalyst's beads. Additionally, 2-propanol modifies the secondary structure of the enzyme by decreasing the β-sheet contribution and increasing the β-turn structure. The molecular modeling of the interaction of R/S-ketoprofen and 2-propanol with the catalytic triad of the lipase provides evidences that the secondary alcohol exerts an important steric hindrance for the reaction to proceed.

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