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1111790-40-9

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1111790-40-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1111790-40-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,1,1,7,9 and 0 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1111790-40:
(9*1)+(8*1)+(7*1)+(6*1)+(5*7)+(4*9)+(3*0)+(2*4)+(1*0)=109
109 % 10 = 9
So 1111790-40-9 is a valid CAS Registry Number.

1111790-40-9Downstream Products

1111790-40-9Relevant academic research and scientific papers

Cobalt(II) amido complexes derived from a monodentate arylamido ligand featuring a highly electron-withdrawing C6F5 substituent

Yao, Shuang,Tam, Dennis Yiu Sun,Cheung, Pak Shing,Lam, Chi-Keung,Guo, Pei,Lam, Sik Lok,Lee, Hung Kay

, p. 17950 - 17959 (2015)

A series of cobalt(ii) complexes of a highly electron-withdrawing amido ligand, [N(C6F5)(C6H3Pri2-2,6)]- (L), were synthesized and structurally characterized. Mononuclear [CoL(Cl)(TMEDA)] (3) and heterobimetallic [CoL2(μ-Cl)Li(THF)3] (4) were obtained by direct metathetical reactions of anhydrous CoCl2 with one molar equivalent of [LiL(TMEDA)] (1) (TMEDA = Me2NCH2CH2NMe2) and [LiL(THF)3] (2), respectively. Complex 3 underwent facile ligand substitution reactions with LiMe and NaN3, yielding the corresponding mixed-ligand complexes [CoL(X)(TMEDA)] (X = Me 5, N36). Treatment of 3 with NaOMe led to the heterobimetallic complex [CoL2(μ-OMe)Na(TMEDA)] (7). The solid-state structures of complexes 1-7 were established by X-ray diffraction analysis.

Copper(II) acetate catalyzed cross-coupling of pentafluorophenylboronic acid with amines under an atmosphere of oxygen

Zhong, Weihui,Liu, Zhenyu,Yu, Chuanming,Su, Weike

experimental part, p. 2888 - 2892 (2009/05/07)

Under an atmosphere of oxygen and a catalytic amount of Cu(OAc) 2, pentafluorophenylboronic acid reacted with anilines at room temperature to produce the corresponding N-pentafluorophenylanilines in moderate to good yields. In the case of alkylamines, unexpected N-alkyl-2,2′,3, 3′,4′,5,5′,6,6′-nona-fluorobiphenyl-4-amines were formed under the similar conditions in moderate yields. Georg Thieme Verlag Stuttgart.

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