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1373752-28-3

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1373752-28-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1373752-28-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,7,3,7,5 and 2 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1373752-28:
(9*1)+(8*3)+(7*7)+(6*3)+(5*7)+(4*5)+(3*2)+(2*2)+(1*8)=173
173 % 10 = 3
So 1373752-28-3 is a valid CAS Registry Number.

1373752-28-3Downstream Products

1373752-28-3Relevant academic research and scientific papers

A novel GPER antagonist protects against the formation of estrogen-induced cholesterol gallstones in female mice

Arnatt, Christopher K.,Arnett, Stacy,Cole, Aidan,DeLeon, Chelsea,Gunn, Joseph,Wang, David Q.-H.,Wang, Helen H.,Wilhelm, McKenna

, p. 767 - 777 (2020/06/01)

Many clinical studies and epidemiological investigations have clearly demonstrated that women are twice as likely to develop cholesterol gallstones as men, and oral contraceptives and other estrogen therapies dramatically increase that risk. Further, anim

Palladium-catalyzed direct coupling of 2-vinylanilines and isocyanides: An efficient synthesis of 2-aminoquinolines

Wang, Lijie,Ferguson, Jamie,Zeng, Fanlong

supporting information, p. 11486 - 11491 (2015/12/04)

Palladium-catalyzed oxidative coupling of 2-vinylanilines and isocyanides constitutes a direct, facile, and efficient approach to 2-aminoquinolines. The procedure, employing palladium acetate and silver carbonate, is attractive in terms of assembly efficiency, functional group tolerance, and operational simplicity. A variety of 2-aminoquinolines were prepared in good to excellent yields.

Rh2(II)-catalyzed intramolecular aliphatic C-H bond amination reactions using aryl azides as the N-atom source

Nguyen, Quyen,Sun, Ke,Driver, Tom G.

supporting information; experimental part, p. 7262 - 7265 (2012/06/16)

Rhodium(II) dicarboxylate complexes were discovered to catalyze the intramolecular amination of unactivated primary, secondary, or tertiary aliphatic C-H bonds using aryl azides as the N-atom precursor. While a strong electron-withdrawing group on the nitrogen atom is typically required to achieve this reaction, we found that both electron-rich and electron-poor aryl azides are efficient sources for the metal nitrene reactive intermediate.

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