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(Z)-3-Furan-2-yl-3-phenyl-acrylic acid ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

59562-36-6

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59562-36-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 59562-36-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,5,6 and 2 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 59562-36:
(7*5)+(6*9)+(5*5)+(4*6)+(3*2)+(2*3)+(1*6)=156
156 % 10 = 6
So 59562-36-6 is a valid CAS Registry Number.

59562-36-6Downstream Products

59562-36-6Relevant academic research and scientific papers

Single-site palladium(II) catalyst for oxidative heck reaction: Catalytic performance and kinetic investigations

Duan, Hui,Li, Menghuan,Zhang, Guanghui,Gallagher, James R.,Huang, Zhiliang,Sun, Yu,Luo, Zhong,Chen, Hongzhong,Miller, Jeffrey T.,Zou, Ruqiang,Lei, Aiwen,Zhao, Yanli

, p. 3752 - 3759 (2015/06/16)

The development of organometallic single-site catalysts (SSCs) has inspired the designs of new heterogeneous catalysts with high efficiency. Nevertheless, the application of SSCs in certain modern organic reactions, such as C-C bond formation reactions, has still been less investigated. In this study, a single-site Pd(II) catalyst was developed, where 2,2′-bipyridine-grafted periodic mesoporous organosilica (PMO) was employed as the support of a Pd(II) complex. The overall performance of the single-site Pd(II) catalyst in the oxidative Heck reaction was then investigated. The investigation results show that the catalyst displays over 99% selectivity for the product formation with high reaction yield. Kinetic profiles further confirm its high catalytic efficiency, showing that the rate constant is nearly 40 times higher than that for the free Pd(II) salt. X-ray absorption spectroscopy reveals that the catalyst has remarkable lifetime and recyclability.

Palladium catalyzed cyclocarbonylation of 3,3-diarylallyl acetates

Iwasaki, Masakazu,Ishii, Youichi,Hidai, Masanobu

, p. 435 - 442 (2007/10/02)

Palladium-catalyzed cyclocarbonylation of 3,3-diarylallyl acetates afforded 4-aryl-substituted 1-naphthyl acetates where the cyclization occurred selectively on the more electron-rich ring.

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