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278790-58-2

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278790-58-2 Usage

Salt form

Imidazole compound

Usage

Pharmaceutical intermediate

Applications

+ Antifungal agent
+ Anti-parasitic agent
+ Chemical intermediate in the synthesis of pharmaceutical drugs
+ Potential use in the treatment of cancer and cardiovascular disease

Usage in organic synthesis

+ Chiral reagent
+ Ligand for metal catalysts

Industries

Pharmaceutical and chemical

Check Digit Verification of cas no

The CAS Registry Mumber 278790-58-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,7,8,7,9 and 0 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 278790-58:
(8*2)+(7*7)+(6*8)+(5*7)+(4*9)+(3*0)+(2*5)+(1*8)=202
202 % 10 = 2
So 278790-58-2 is a valid CAS Registry Number.

278790-58-2Downstream Products

278790-58-2Relevant articles and documents

Basicities and Nucleophilicities of Pyrrolidines and Imidazolidinones Used as Organocatalysts

An, Feng,Maji, Biplab,Min, Elizabeth,Ofial, Armin R.,Mayr, Herbert

supporting information, p. 1526 - 1547 (2020/02/04)

The Br?nsted basicities pKaH (i.e., pKa of the conjugate acids) of 32 pyrrolidines and imidazolidinones, commonly used in organocatalytic reactions, have been determined photometrically in acetonitrile solution using CH acids as indicators. Most investigated pyrrolidines have basicities in the range 16 aH aH aH 12.6) and the 2-imidazoliummethyl-substituted pyrrolidine A21 (pKaH 11.1) are outside the typical range for pyrrolidines with basicities comparable to those of imidazolidinones. Kinetics of the reactions of these 32 organocatalysts with benzhydrylium ions (Ar2CH+) and structurally related quinone methides, common reference electrophiles for quantifying nucleophilic reactivities, have been measured photometrically. Most reactions followed second-order kinetics, first order in amine and first order in electrophile. More complex kinetics were observed for the reactions of imidazolidinones and several pyrrolidines carrying bulky 2-substituents, due to reversibility of the initial attack of the amines at the electrophiles followed by rate-determining deprotonation of the intermediate ammonium ions. In the presence of 2,4,6-collidine or 2,6-di-tert-butyl-4-methyl-pyridine, the deprotonation of the initial adducts became faster, which allowed the rate of the attack of the amines at the electrophiles to be determined. The resulting second-order rate constants k2 followed the correlation log?k2(20 °C) = sN(N + E), where electrophiles are characterized by one parameter (E) and nucleophiles are characterized by the two solvent-dependent parameters N and sN. In this way, the organocatalysts A1-A32 were integrated in our comprehensive nucleophilicity scale, which compares n-, -, and σ-nucleophiles. The nucleophilic reactivities of the title compounds correlate only poorly with their Br?nsted basicities.

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