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102078-89-7

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102078-89-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 102078-89-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,2,0,7 and 8 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 102078-89:
(8*1)+(7*0)+(6*2)+(5*0)+(4*7)+(3*8)+(2*8)+(1*9)=97
97 % 10 = 7
So 102078-89-7 is a valid CAS Registry Number.

102078-89-7Relevant articles and documents

Synthesis of alkynylgold(III) complexes with bis-cyclometalating ligand derived from ethyl 2,6-diphenylisonicotinate and their structural, electrochemical, photo- and electroluminescence studies

Au, Vonika Ka-Man,Tsang, Daniel Ping-Kuen,Wong, Yi-Chun,Chan, Mei-Yee,Yam, Vivian Wing-Wah

, p. 109 - 116 (2015)

Abstract A series of alkynylgold(III) complexes with bis-cyclometalating ligand derived from ethyl 2,6-diphenylisonicotinate has been synthesized. The single crystal structure of one of the complexes revealed an unprecedentedly short Au(III)...Au(III) distance of 3.44 ?. These complexes were found to exhibit rich electrochemistry. Upon photoexcitation, the alkynylgold(III) complexes were found to show rich emission properties in various states at both ambient and low temperatures. One of the complexes have also been utilized as the light-emitting layer in the fabrication of organic light-emitting diodes, demonstrating the potentials and versatility of alkynylgold(III) complexes.

NH4I-Triggered [4 + 2] Annulation of α,β-Unsaturated Ketoxime Acetates with N-Acetyl Enamides for the Synthesis of Pyridines

Duan, Jindian,Zhang, Lei,Xu, Gaochen,Chen, Heming,Ding, Xiaojuan,Mao, Yiyang,Rong, Binsen,Zhu, Ning,Guo, Kai

, p. 8157 - 8165 (2020)

The NH4I-triggered formal [4 + 2] annulation of α,β-unsaturated ketoxime acetates with N-acetyl enamides has been developed. The current protocol employs electron-rich enamides as C2 synthons and enables the efficient and straightforward construction of polysubstituted pyridines in moderate to good yields based on metal-free systems. The reaction tolerates a wide range of functional groups and represents an alternate route toward the synthesis of pyridine derivatives.

Iron-Catalyzed Synthesis of Pyridines from α,β-Unsaturated Ketoxime Acetates and N -Acetyl Enamides

Xu, Gaochen,Yan, Huan,Zhang, Sai,Wu, Qinghuan,Duan, Jindian,Guo, Kai

supporting information, p. 283 - 287 (2021/12/03)

A new method of FeCl2-catalyzed [4+2] annulation of α,β-unsaturated ketoxime acetates with N-acetyl enamides in batch and flow is reported. The current strategy features low-cost catalytic system, use of electron-rich olefins, operational simplicity, and broad substrate scope, thus providing a facile and efficient access to substituted pyridines in moderate to good yields.

Method for synthesizing polysubstituted pyridine from alkenyl azide under catalysis of copper

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Paragraph 0063-0065; 0068; 0070; 0072; 0075; 0077; 0079, (2019/01/07)

The invention provides a method for synthesizing a polysubstituted pyridine compound. The method is characterized in that the compound of formula (I) is synthesized from alkenyl azide or a difluoromethylene compound in a one-step manner under the catalysi

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