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1264932-10-6

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1264932-10-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1264932-10-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,6,4,9,3 and 2 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1264932-10:
(9*1)+(8*2)+(7*6)+(6*4)+(5*9)+(4*3)+(3*2)+(2*1)+(1*0)=156
156 % 10 = 6
So 1264932-10-6 is a valid CAS Registry Number.

1264932-10-6Downstream Products

1264932-10-6Relevant articles and documents

Building a Pyrazole–Benzothiadiazole–Pyrazole Photosensitizer into Metal–Organic Frameworks for Photocatalytic Aerobic Oxidation

Jin, Ji-Kang,Wu, Kun,Liu, Xin-Yi,Huang, Guo-Quan,Huang, Yong-Liang,Luo, Dong,Xie, Mo,Zhao, Yifang,Lu, Weigang,Zhou, Xiao-Ping,He, Jian,Li, Dan

supporting information, p. 21340 - 21349 (2021/12/17)

Charge separation plays a crucial role in regulating photochemical properties and therefore warrants consideration in designing photocatalysts. Metal–organic frameworks (MOFs) are emerging as promising candidates for heterogeneous photocatalysis due to their structural designability and tunability of photon absorption. Herein, we report the design of a pyrazole–benzothiadiazole–pyrazole organic molecule bearing a donor–acceptor–donor conjugated π-system for fast charge separation. Further attempts to integrate such a photosensitizer into MOFs afford a more effective heterogeneous photocatalyst (JNU-204). Under visible-light irradiation, three aerobic oxidation reactions involving different oxygenation pathways were achieved on JNU-204. Recycling experiments were conducted to demonstrate the stability and reusability of JNU-204 as a robust heterogeneous photocatalyst. Furthermore, we illustrate its applications in the facile synthesis of pyrrolo[2,1-a]isoquinoline-containing heterocycles, core skeletons of a family of marine natural products. JNU-204 is an exemplary MOF platform with good photon absorption, suitable band gap, fast charge separation, and extraordinary chemical stability for proceeding with aerobic oxidation reactions under visible-light irradiation.

Pyrrole [2,1-a] isoquinoline alkaloid and preparation method and application thereof

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Paragraph 0057; 0064; 0065; 0066, (2018/03/24)

The invention discloses pyrrole [2,1-a] isoquinoline alkaloid and a preparation method and medical application thereof, and belongs to the field of medicinal chemistry. The structural general formula of the pyrrole [2,1-a] isoquinoline alkaloid is as show

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