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3-ethoxy-2-phenyl-2-cyclohexen-1-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

73960-97-1

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73960-97-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 73960-97-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,9,6 and 0 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 73960-97:
(7*7)+(6*3)+(5*9)+(4*6)+(3*0)+(2*9)+(1*7)=161
161 % 10 = 1
So 73960-97-1 is a valid CAS Registry Number.

73960-97-1Relevant academic research and scientific papers

Asymmetric Hydrogenation of Racemic 6-Aryl 1,4-Dioxaspiro[4.5]decan-7-ones to Functionalized Chiral ?a'Aryl Cyclohexanols via a Dynamic Kinetic Resolution

Yang, Dan,Yang, Ai-Jiao,Chen, Yong,Xie, Jian-Hua,Zhou, Qi-Lin

supporting information, p. 1616 - 1620 (2021/03/03)

A ruthenium-catalyzed asymmetric hydrogenation method for the synthesis of functionalized β-aryl cyclohexanols is described. With chiral spiro ruthenium catalyst (Ra,S,S)-5c, a series of racemic α-aryl cyclohexanones bearing a β-monoethylene ketal group were hydrogenated to the corresponding functionalized β-aryl cyclohexanols in high yields with enantioselectivity of up to 99% ee via a dynamic kinetic resolution. This protocol can be conducted on a decagram scale and provide potential approaches for the synthesis of optically active and densely functionalized aryl cyclohexanols.

Asymmetric synthesis of 1,2,3-trisubstituted cyclopentanes and cyclohexanes as key components of substance P antagonists

Kuethe, Jeffrey T.,Wong, Audrey,Wu, Jimmy,Davies, Ian W.,Dormer, Peter G.,Welch, Christopher J.,Hillier, Michael C.,Hughes, David L.,Reider, Paul J.

, p. 5993 - 6000 (2007/10/03)

An efficient asymmetric synthesis of 1,2,3-trisubstituted cyclopentanes and cyclohexanes is described. Three methods were developed for the preparation of the 2,3-disubstituted cyclopentenones and cyclohexenones, which are key achiral building blocks. These intermediates are reduced catalytically with (R)-2-methyloxazaborolidine in high yield (82-98%) and excellent ee (89-96%). Directed reduction of the chiral allylic alcohols using Red-Al gives exclusively the 1,2-anti stereochemistry (>99:1). Epimerization of the ester center followed by saponification/crystallization affords the desired hydroxyacids in good yield (65-70%) and in high enantiomeric excess (>99%).

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