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18513-01-4

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18513-01-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 18513-01-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,5,1 and 3 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 18513-01:
(7*1)+(6*8)+(5*5)+(4*1)+(3*3)+(2*0)+(1*1)=94
94 % 10 = 4
So 18513-01-4 is a valid CAS Registry Number.

18513-01-4Relevant academic research and scientific papers

Organocatalytic Direct N-Acylation of Amides with Aldehydes under Oxidative Conditions

Zheng, Chenguang,Liu, Xiang,Ma, Cheng

, p. 6940 - 6945 (2017/07/13)

The direct oxidative N-acylation reaction of primary amides with aryl/α,β-unsaturated aldehydes was achieved in the presence of azolium salt C3 and an inorganic base using 3,3′,5,5′-tetra-tert-butyldiphenoquinone as the oxidant, thus providing an efficient approach for the synthesis of three types of imide compounds including N-sulfonylcarboxamides, N-sulfinylcarboxamides, and dicarboxyimides in good yield.

Synthesis and arylation of unprotected sulfonimidamides

Funes Maldonado, Matías,Sehgelmeble, Fernando,Bjarnemark, Fanny,Svensson, Mats,?hman, Jens,Arvidsson, Per I.

experimental part, p. 7456 - 7462 (2012/09/22)

Herein we evaluate different methodologies for the synthesis of unprotected sulfonimidamides. Three different procedures that allow orthogonal deprotection of the imine nitrogen under acidic, nucleophilic, and basic conditions were established. Moreover,

Synthesis of CF3-substituted sulfoximines from sulfonimidoyl fluorides

Kowalczyk, Rafal,Edmunds, Andrew J. F.,Hall, Roger G.,Bolm, Carsten

supporting information; experimental part, p. 768 - 771 (2011/04/24)

N-Protected trifluoromethyl-substituted sulfoximines have been prepared by treatment of sulfonimidoyl fluorides with a combination of the Ruppert-Prakash reagent (TMSCF3) and tetrabutyl ammonium fluoride (TBAF). The starting materials were accessed following two synthetic routes, and for each reaction sequence the substrate scope was evaluated. Accordingly, a wide variety of aryl-substituted products were obtained in moderate to good yield.

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