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16764-90-2

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16764-90-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 16764-90-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,7,6 and 4 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 16764-90:
(7*1)+(6*6)+(5*7)+(4*6)+(3*4)+(2*9)+(1*0)=132
132 % 10 = 2
So 16764-90-2 is a valid CAS Registry Number.

16764-90-2Relevant academic research and scientific papers

Cr, Zr-incorporated hydrotalcites and their application in the synthesis of isophorone

Liu, Yanxia,Sun, Kunpeng,Ma, Haowen,Xu, Xianlun,Wang, Xiaolai

, p. 880 - 883 (2010)

Cr3+ and Zr4+ cation-incorporated hydrotalcites (HTs) were prepared by coprecipitation method. Corresponding mixed oxide were obtained by the thermal decomposition of HTs at 773 K for 8 h and applied in the synthesis of isophorone (IP) from acetone. From the characteristic results, both Cr3+ and Zr4+ were introduced into the lattice of hydrotalcite producing the more disordered HT structures. Compared with Mg-Al mixed oxide, Cr and Zr modified mixed oxide demonstrated more amount of basic sites and stronger base strength, which were responsible for the improvement of catalytic activity. As a result, both of the modified mixed oxide exhibited IP selectivity of more than 70% under atmospheric pressure.

Copper(II)-Catalyzed Tandem Decarboxylative Michael/Aldol Reactions Leading to the Formation of Functionalized Cyclohexenones

Lee, Jeonghyo,Wang, Sibin,Callahan, Miranda,Nagorny, Pavel

supporting information, p. 2067 - 2070 (2018/04/16)

This work describes the development of a new single-pot copper(II)-catalyzed decarboxylative Michael reaction between β-keto acids and enones, followed by in situ aldolization, which results in highly functionalized chiral and achiral cyclohexenones. The achiral version of this Robinson annulation features a hitherto unprecedented Michael reaction of β-keto acids with sterically hindered β,β′-substituted enones and provides access to all carbon quaternary stereocenter-containing cyclohexenones (11 examples, 43-83% yield). In addition, an asymmetric chiral bis(oxazoline) copper(II)-catalyzed single-pot Robinson annulation has been devised for preparing chiral cyclohexenones, including some products that contain vicinal stereocenters (5 examples, 65-85% yield, 84-94% ee). This latter protocol has been successfully applied to the enantioselective formation of the oxygenated 10-nor-steroid core from readily available starting materials.

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