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(S)-2-octyl laurate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

172719-82-3

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172719-82-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 172719-82-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,2,7,1 and 9 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 172719-82:
(8*1)+(7*7)+(6*2)+(5*7)+(4*1)+(3*9)+(2*8)+(1*2)=153
153 % 10 = 3
So 172719-82-3 is a valid CAS Registry Number.

172719-82-3Downstream Products

172719-82-3Relevant academic research and scientific papers

Continuous Flow Enzymatic Kinetic Resolution and Enantiomer Separation using Ionic Liquid/Supercritical Carbon Dioxide Media

Reetz, Manfred T.,Wiesenhoefer, Wolfgang,Francio, Giancarlo,Leitner, Walter

, p. 1221 - 1228 (2003)

The combination of kinetic resolution in ionic liquids (IL) and selective extraction with supercritical carbon dioxide (scCO2) provides a new approach for the separation of enantiomers as exemplified by the lipase-catalyzed esterification of chiral secondary alcohols. Excellent enantioselectivities are achieved upon conversion of alcohols 1a-e to the corresponding acetates 4a-e or laureates 5a-e using various modifications of the lipase from Candida antarctica (CaL-B) in imidazolium-based ionic liquids. The anion of the ionic liquid has a significant influence on the performance of the bio-catalyst with bis(trifluoromethanesulfonamide) [BTA] giving the best results. The acetates 4a-e can be extracted from the reaction mixture preferentially over the alcohols 1a-e with scCO2 under certain conditions, but preparatively useful selectivities would require advanced multi-step extraction procedures. In contrast, efficient separation is possible with relatively simple equipment if alcohols 1a-e are extracted preferentially from their corresponding laureates 5a-e. A "green" continuous process for the resolution of racemic alcohols without the use of organic solvents was devised on the basis of these findings.

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