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211449-24-0

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211449-24-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 211449-24-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,1,4,4 and 9 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 211449-24:
(8*2)+(7*1)+(6*1)+(5*4)+(4*4)+(3*9)+(2*2)+(1*4)=100
100 % 10 = 0
So 211449-24-0 is a valid CAS Registry Number.

211449-24-0Relevant articles and documents

Corrigendum to “Copper ferrite superparamagnetic nanoparticles as a heterogeneous catalyst for directed phenol/formamide coupling” [Tetrahedron Lett. 58 (2017) 3370–3373] (Tetrahedron Letters (2017) 58(34) (3370–3373), (S0040403917309048), (10.1016/j.tetl

Le, Dung T.,Nguyen, Chung K.,Nguyen, Ngon N.,Nguyen, Tung T.,Nguyen, Viet D.,Phan, Nam T. S.,Tran, Kien N.

, (2021)

The authors regret that some characterization images of the catalyst and some NMR data of the compounds in Table 2 were shown incorrectly in the Supplementary Data. The coupling reactions were therefore re-run using the reported procedure and isolation of

Directed ortho-Metalation of O-Aryl N,N-Dialkylcarbamates: Methodology, Anionic ortho-Fries Rearrangement, and Lateral Metalation

Miah, M. A. Jalil,Sibi, Mukund P.,Chattopadhyay,Familoni, Oluwole B.,Snieckus, Victor

, p. 440 - 446 (2017/12/15)

The directed ortho-lithiation reactions of O-aryl N,N-dialkylcarbamates as well as O-1-naphthyl and O-2-naphthyl N,N-dialkylcarbamates with sec-butyllithium/tetramethylethylenediamine (sBuLi/TMEDA) followed by quenching with various electrophiles afford a range of polysubstituted aromatic compounds. If the solutions of the ortho-lithiated carbamates are warmed to room temperature without the addition of external electrophiles, salicylamide and 1- and 2-hydroxynaphthamide derivatives are formed through anionic ortho-Fries rearrangements. The relative stabilities and reactivities of different O-aryl N,N-dialkylcarbamates were investigated. The lateral metalation of 2-tolyl carbamates with lithium diisopropylamide (LDA) provides a route to benzo[b]furan-2(3H)-ones. Previously reported results are used in a comparison of seven O-based directed metalation groups in reactions with several electrophiles. The described methodology is useful for the preparation of 1,2,3-substituted aromatic compounds.

Nickel-catalyzed oxidative esterification of formamides with 1,3-dicarbonyl compounds under mild reaction conditions

Saberi, Dariush,Poorsadeghi, Samira

, (2017/09/30)

Synthesis of enol carbamates was achieved via nickel-catalyzed oxidative coupling of formamides with 1,3-dicarbonyl compounds in the presence of tert-butyl hydroperoxide at 40?°C. Various derivatives of enol carbamates were synthesized by this method in good to excellent yields.

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