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27721-47-7

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27721-47-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 27721-47-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,7,7,2 and 1 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 27721-47:
(7*2)+(6*7)+(5*7)+(4*2)+(3*1)+(2*4)+(1*7)=117
117 % 10 = 7
So 27721-47-7 is a valid CAS Registry Number.

27721-47-7Relevant articles and documents

Metal-free aerobic oxidative coupling of amines in dimethyl sulfoxide via a radical pathway

Lin, Mu,Wang, Zikuan,Fang, Huayi,Liu, Lianghui,Yin, Haolin,Yan, Chun-Hua,Fu, Xuefeng

, p. 10861 - 10864 (2016)

Metal-free oxidative coupling of amines is achieved simply by heating their dimethyl sulfoxide (DMSO) solution under oxygen as oxidant without any other catalysts or additives, accompanied by the formation of an equimolar amount of dimethyl sulfone (DMSO2). EPR experiments indicate that the reaction proceeds via a radical pathway. DMSO may play a triple role as solvent, radical initiator and co-reductant.

Unusually Reactive Cyclic Anhydride Expands the Scope of the Castagnoli-Cushman Reaction

Chizhova, Maria,Khoroshilova, Olesya,Dar'In, Dmitry,Krasavin, Mikhail

, p. 12722 - 12733 (2018/10/15)

In the course of synthesizing and testing various "azole-including" cyclic anhydrides in the Castagnoli-Cushman reaction with imines, a remarkably reactive, pyrrole-based anhydride has been identified. It displayed a remarkably efficient reaction with N-alkyl and N-aryl imines, in particular, with "enolizable" α-C-H imines which typically fail to react with a majority of known cyclic anhydrides. The reactivity of this anhydride has been justified by an efficient resonance stabilization of its enol form. This finding expands the existing arsenal of highly reactive cyclic anhydrides and further confirms the importance of anhydride enolization for an efficient Castagnoli-Cushman reaction.

General and selective reductive amination of carbonyl compounds using a core-shell structured Co3O4/NGr@C catalyst

Stemmler, Tobias,Westerhaus, Felix A.,Surkus, Annette-Enrica,Pohl, Marga-Martina,Junge, Kathrin,Beller, Matthias

, p. 4535 - 4540 (2014/12/10)

The application of heterogenized non-noble metal-based catalysts in selective catalytic hydrogenation processes is still challenging. In this respect, the preparation of a well-defined cobalt-based catalyst was investigated by immobilization of the corresponding cobalt(ii)-phenanthroline-chelate on Vulcan XC72R carbon powder. The formed core-shell structured cobalt/cobalt oxide nanocomposites are encapsulated by nitrogen-enriched graphene layers. This promising cheap heterogeneous catalyst allows for an efficient domino reductive amination of carbonyl compounds with nitroarenes. This journal is

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