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117266-97-4

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117266-97-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 117266-97-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,7,2,6 and 6 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 117266-97:
(8*1)+(7*1)+(6*7)+(5*2)+(4*6)+(3*6)+(2*9)+(1*7)=134
134 % 10 = 4
So 117266-97-4 is a valid CAS Registry Number.

117266-97-4Relevant articles and documents

PHOTOLYSIS OF THE AZOALKANE 2,3-DIAZATRICYCLO4,9>NON-2-ENE: DIRECT OBSERVATION OF 4-CYCLOHEXENYLDIAZOMETHANE

Adam, Waldemar,Carballeira, Nestor,Gillaspey, William D.

, p. 5473 - 5476 (1983)

Besides denitrogenation to the tricycloalkane 8, the photolysis of azoalkane 3 affords the diazoalkane 4, which serves as precursor to the minor hydrocarbon products 9, 10 and 11; irradiation of azoalkane 3 with the 333.6 nm line of an 18-W argon ion laser was essential to obtain preparative quantities of diazoalkane 4 for its detection and identification.

Amide/Iminium Zwitterionic Catalysts for (Trans)esterification: Application in Biodiesel Synthesis

Lam, Ying-Pong,Ng, Wing-Hin,Tan, Fei,Tse, Ying-Lung Steve,Wang, Xinyan,Yeung, Ying-Yeung

, p. 8083 - 8092 (2019/08/26)

A class of zwitterionic organocatalysts based on an amide anion/iminium cation charge pair has been developed. The zwitterions are easily prepared by reacting aziridines with aminopyridines. They are catalytically applicable to transesterifications and dehydrative esterifications. Mechanistic studies reveal that the amide anion and iminium cation work synergistically in activating the reaction partners, with the iminium cationic moiety interacting with the carbonyl substrates through nonclassical hydrogen bonding. The reaction can be applied to large-scale synthesis of biodiesel under mild conditions.

A fast and practical approach to tetrahydropyranylation and depyranylation of alcohols using indium triflate

Mineno, Tomoko

, p. 7975 - 7978 (2007/10/03)

Indium triflate-mediated tetrahydropyranylation of alcohols in dichloromethane and depyranylation of these products in aqueous methanol utilizing the same reagent but different molar ratio is described. In addition, indium triflate-promoted conversion of tetrahydropyran ethers to their corresponding acetates has also been described.

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