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54353-98-9

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54353-98-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 54353-98-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,3,5 and 3 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 54353-98:
(7*5)+(6*4)+(5*3)+(4*5)+(3*3)+(2*9)+(1*8)=129
129 % 10 = 9
So 54353-98-9 is a valid CAS Registry Number.

54353-98-9Downstream Products

54353-98-9Relevant academic research and scientific papers

Catalytic, Enantioselective β-Protonation through a Cooperative Activation Strategy

Wang, Michael H.,Barsoum, David,Schwamb, C. Benjamin,Cohen, Daniel T.,Goess, Brian C.,Riedrich, Matthias,Chan, Audrey,Maki, Brooks E.,Mishra, Rama K.,Scheidt, Karl A.

, p. 4689 - 4702 (2017)

The NHC-catalyzed transformation of unsaturated aldehydes into saturated esters through an organocatalytic homoenolate process has been thoroughly studied. Leveraging a unique “Umpolung”-mediated β-protonation, this process has evolved from a test bed for homoenolate reactivity to a broader platform for asymmetric catalysis. Inspired by our success in using the β-protonation process to generate enals from ynals with good E/Z selectivity, our early studies found that an asymmetric variation of this reaction was not only feasible, but also adaptable to a kinetic resolution of secondary alcohols through NHC-catalyzed acylation. In-depth analysis of this process determined that careful catalyst and solvent pairing is critical for optimal yield and selectivity; proper choice of nonpolar solvent provided improved yield through suppression of an oxidative side reaction, while employment of a cooperative catalytic approach through inclusion of a hydrogen bond donor cocatalyst significantly improved enantioselectivity.

Palladium-catalyzed double arylations of terminal olefins in acetic acid

Xu, Daichao,Lu, Chunxin,Chen, Wanzhi

experimental part, p. 1466 - 1474 (2012/03/08)

A palladium-catalyzed Heck diarylation of terminal olefins under ligand-free conditions in acetic acid is described. This procedure allows double arylation of terminal olefins affording trisubstituted olefins in good to excellent yields. The methodology is applicable to the coupling of both electron-deficient and electron-rich aryl iodides leading to symmetrical and unsymmetrical β,β-diarylated alkenes.

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