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syn-(1,1-dimethylethyl) 3-hydroxy-2-methyl-5-phenyl-4-pentenethioate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

97250-92-5

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97250-92-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 97250-92-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,7,2,5 and 0 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 97250-92:
(7*9)+(6*7)+(5*2)+(4*5)+(3*0)+(2*9)+(1*2)=155
155 % 10 = 5
So 97250-92-5 is a valid CAS Registry Number.

97250-92-5Downstream Products

97250-92-5Relevant academic research and scientific papers

Chemistry of enoxysilacyclobutanes: Highly selective uncatalyzed aldol additions

Denmark, Scott E.,Griedel, Brian D.,Coe, Diane M.,Schnute, Mark E.

, p. 7026 - 7043 (2007/10/02)

O-(Silacyclobutyl) ketene acetals derived from esters, thiol esters, and amides underwent facile aldol addition with a variety of aldehydes at room temperature without the need for catalysts. The uncatalyzed aldol addition reaction of O-(silacyclobutyl) ketene acetals displayed the following characteristics: (1) the rate of reaction was highly dependent on the spectator substituent on silicon and the geometry of the ketene acetal, (2) the O,O-ketene acetal of E configuration afforded the syn aldol products with high diastereoselectivity (93/7 to 99/1), (3) conjugated aldehydes reacted more rapidly than aliphatic aldehydes, and (4) the reaction was mildly sensitive to solvent. In addition, the aldol reaction was found to be efficiently catalyzed by metal alkoxides. Labeling experiments revealed that the thermal aldol reaction proceeds by direct intramolecular silicon group transfer, while the alkoxide-catalyzed version probably proceeds via in situ generated metal enolates. Computational modeling of the transition states suggests that the boat transition structures are preferred, supporting the observed syn selectivity of the thermal aldol reaction. Both thermal and alkoxide-catalyzed Michael additions were investigated, revealing a competition between 1,2- and 1,4-addition favoring the former.

LEWIS ACID MEDIATED ALDOL CONDENSATIONS USING THIOESTER SILYL KETENE ACETALS

Gennari, Cesare,Beretta, M. Grazia,Bernardi, Anna,Moro, Giorgio,Scolastico, Carlo,Todeschini, Roberto

, p. 893 - 910 (2007/10/02)

BF3-OEt2 mediated thioester silylketene acetal additions to aldehydes are stereoconvergent and give high anti-syn ratios and good chemical yields.An acyclic transition state model was hypothesized in order to account for the observed selectivity.Theoretic

HIGH DIASTEREOSELECTIVITY IN LEWIS ACID MEDIATED ALDOL CONDENSATIONS USING THIOESTER SILYL KETENE ACETALS.

Gennari, Cesare,Bernardi, Anna,Cardani, Silvia,Scolastico, Carlo

, p. 797 - 800 (2007/10/02)

BF3OEt2 mediated aldol condensations of thioester silyl ketene acetals are stereoconvergent, and exhibit high internal (anti) and relative (Cram) diastereoselectivity.

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