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1-{2-[6-(tert-butyl-diphenyl-silanyloxymethyl)-2,2-dimethyl-tetrahydro-furo[3,4-d][1,3]dioxol-4-yl]-isoxazolidin-5-yl}-5-methyl-1H-pyrimidine-2,4-dione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

290293-17-3

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  • 1-{2-[6-(tert-butyl-diphenyl-silanyloxymethyl)-2,2-dimethyl-tetrahydro-furo[3,4-d][1,3]dioxol-4-yl]-isoxazolidin-5-yl}-5-methyl-1H-pyrimidine-2,4-dione

    Cas No: 290293-17-3

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290293-17-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 290293-17-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,9,0,2,9 and 3 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 290293-17:
(8*2)+(7*9)+(6*0)+(5*2)+(4*9)+(3*3)+(2*1)+(1*7)=143
143 % 10 = 3
So 290293-17-3 is a valid CAS Registry Number.

290293-17-3Downstream Products

290293-17-3Relevant articles and documents

Enantioselective syntheses and cytotoxicity of N,O-nucleosides

Chiacchio, Ugo,Corsaro, Antonino,Iannazzo, Daniela,Piperno, Anna,Pistarà, Venerando,Rescifina, Antonio,Romeo, Roberto,Valveri, Vincenza,Mastino, Antonio,Romeo, Giovanni

, p. 3696 - 3702 (2007/10/03)

Enantiomers of 4′-aza-2′,3′-dideoxynucleosides have been prepared by two different synthetic approaches, on the basis of 1,3-dipolar cycloaddition of a chiral nitrone. Cytotoxicity and apoptotic activity have been investigated. (5′S)-5-Fluoro-1-isoxazolid

Diastereoselective and enantioselective synthesis of 4'-aza analogues of 2',3'-dideoxynucleosides

Chiacchio, Ugo,Rescifina, Antonio,Corsaro, Antonio,Pistara, Venerando,Romeo, Giovanni,Romeo, Roberto

, p. 2045 - 2048 (2007/10/03)

A diastereo- and enantioselective synthesis of 4'-aza analogues of 2',3'-dideoxynucleosides has been designed by the strategy of the 1,3-dipolar cycloaddition reaction of a Vasella-type nitrone. The reaction leads to (1'R)- and (1'S)-4'-aza analogues of 2',3'-dideoxythimidine and fluorouridine, in enantiomerically pure forms. Copyright (C) 2000 Elsevier Science Ltd.

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