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S-di(11-hydroxyundecyl)-1-phenylethylammonium bromide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1600533-94-5

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1600533-94-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1600533-94-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,0,0,5,3 and 3 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1600533-94:
(9*1)+(8*6)+(7*0)+(6*0)+(5*5)+(4*3)+(3*3)+(2*9)+(1*4)=125
125 % 10 = 5
So 1600533-94-5 is a valid CAS Registry Number.

1600533-94-5Downstream Products

1600533-94-5Relevant academic research and scientific papers

Polyoxometalate complexes for oxidative kinetic resolution of secondary alcohols: Unique effects of chiral environment, immobilization and aggregation

Shi, Lei,Wang, Yizhan,Li, Bao,Wu, Lixin

, p. 9177 - 9188 (2014)

In this paper, the chiral surfactants bearing two long alkyl chains with hydroxyl groups at their terminals were synthesized and employed to encapsulate a catalytically efficient polyoxometalate through electrostatic interaction. The obtained chiral surfactant-encapsulated polyoxometalate complexes, in which a defined chiral microenvironment surrounds the inorganic cluster, were covalently immobilized into the silica matrix via a sol-gel process. Kinetic resolution of racemic aromatic alcohols was selected as the model reaction to evaluate the chiral supramolecular hybrid catalysts. Up to 89% enantiomeric excess was obtained by varying the reaction conditions. Importantly, the change of loading values of the chiral surfactant-encapsulated polyoxometalates leads to mutative inner microstructures ranging from uniform dispersion to subsequent formation of nanocrystalline domains in the silica matrix. Such a structural evolution differentiates the density and stability of the chiral microenvironment, resulting in a regular change of enantioselectivity of the prepared asymmetric catalysts. Moreover, the fixation of the chiral microenvironment surrounding the polyoxometalates by covalent immobilization was proved to have a promoting effect on enantioselectivity. The present research uncovers the unique effect of immobilization on the kinetic resolution. The strategy helps to understand the influencing factors of enantioselectivity, and provides a convenient and efficient approach for the construction of supramolecular asymmetric catalysts based on chiral surfactant-encapsulated polyoxometalate complexes. the Partner Organisations 2014.

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