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cis-syn-cis-10-phenylperhydroacridine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

114544-16-0

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114544-16-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 114544-16-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,4,5,4 and 4 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 114544-16:
(8*1)+(7*1)+(6*4)+(5*5)+(4*4)+(3*4)+(2*1)+(1*6)=100
100 % 10 = 0
So 114544-16-0 is a valid CAS Registry Number.

114544-16-0Downstream Products

114544-16-0Relevant academic research and scientific papers

Saturated nitrogen-containing heterocycles. 19. Catalytic reduction of 10- and 9,10-substituted sym-octahydroacridinium salts

Seller,Reshetov,Seller,Kriven'ko

, p. 971 - 974 (2007/10/03)

10-Methyl(phenyl)- and 9,10-diphenylperhydroacridines have been obtained by the catalytic reduction of 10- and 9,10-substituted sym-octahydroacridinium salts. Selective reduction of the furan ring occurred in the case of 9-(2-furyl)-10-phenyl-sym-octahydroacridinium perchlorate. The stereoisomeric composition of the reaction products has been established and a probable scheme for their formation has been proposed.

SATURATED NITROGEN-CONTAINING HETEROCYCLES. 16. CATALYTIC SYNTHESIS OF N-ARYLPERHYDROACRIDINES

Nikolaeva, T. G.,Yudovich, L. M.,Komyagin, N. T.,Yanovskii, A. I.,Struchkov, Yu. T.,Kriven'ko, A. P.

, p. 932 - 937 (2007/10/02)

Catalytic hydrogenation of methylene-2,2'-dicyclohexanone in the presence of substituted anilines or nitrobenzenes involves the formation of N-arylperhydroacridines. The stereoisomeric composition and yields of the latter are determined by the nature and

SATURATED NITROGEN-CONTAINING HETEROCYCLES. 13. PERHYDROACRIDINES. SYNTHESIS AND STEREOCHEMISTRY

Kriven'ko, A. P.,Nikolaeva, T. G.,Yudovich, L. M.,Komyagin, N. T.,Yanovskii, A. I.,et al.

, p. 1324 - 1329 (2007/10/02)

The configurations of the perhydroacridines formed in the catalytic hydroamination of threo-methylenedicyclohexanone and the product of its cyclization - 2-hydroxy-2,3-tetramethylenebicyclononan-9-one - were established by means of the 13C NMR spectra and alternative synthesis.It is shown that isomers with cis-anti-cis and cis-syn-cis configurations are formed as a result of the reactions.The results of X-ray diffraction analysis are presented for cis-syn-cis-N-(2-hydroxyethyl)perhydroacridine.

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