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1,2-Dioxolan-3-ol, 3,5,5-trimethyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

19789-15-2

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19789-15-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 19789-15-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,7,8 and 9 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 19789-15:
(7*1)+(6*9)+(5*7)+(4*8)+(3*9)+(2*1)+(1*5)=162
162 % 10 = 2
So 19789-15-2 is a valid CAS Registry Number.

19789-15-2Upstream product

19789-15-2Downstream Products

19789-15-2Relevant academic research and scientific papers

Hydrotalcite-Promoted Epoxidation of Electron-Deficient Alkenes with Hydrogen Peroxide

Cativiela, Carlos,Figueras, Francois,Fraile, Jose M.,Garcia, Jose I.,Mayoral, Jose A.

, p. 4125 - 4128 (1995)

A synthetic anionic clay, hydrotalcite (Mg/Al=2.8), promotes the epoxidation of electrondeficient alkenes with H2O2.With open-chain, α,β-unsaturated carbonyl compounds 3-hydroxy-1,2-dioxolanes are also obtained.

The cinchona primary amine-catalyzed asymmetric epoxidation and hydroperoxidation of α,β-unsaturated carbonyl compounds with hydrogen peroxide

Lifchits, Olga,Mahlau, Manuel,Reisinger, Corinna M.,Lee, Anna,Fares, Christophe,Polyak, Iakov,Gopakumar, Gopinadhanpillai,Thiel, Walter,List, Benjamin

supporting information, p. 6677 - 6693 (2013/06/05)

Using cinchona alkaloid-derived primary amines as catalysts and aqueous hydrogen peroxide as the oxidant, we have developed highly enantioselective Weitz-Scheffer-type epoxidation and hydroperoxidation reactions of α,β-unsaturated carbonyl compounds (up to 99.5:0.5 er). In this article, we present our full studies on this family of reactions, employing acyclic enones, 5-15-membered cyclic enones, and α-branched enals as substrates. In addition to an expanded scope, synthetic applications of the products are presented. We also report detailed mechanistic investigations of the catalytic intermediates, structure-activity relationships of the cinchona amine catalyst, and rationalization of the absolute stereoselectivity by NMR spectroscopic studies and DFT calculations.

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