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(4R,5R)-5-Ethyl-4-hydroxy-5-hydroxymethyl-dihydro-furan-2-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

869210-33-3

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869210-33-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 869210-33-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,9,2,1 and 0 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 869210-33:
(8*8)+(7*6)+(6*9)+(5*2)+(4*1)+(3*0)+(2*3)+(1*3)=183
183 % 10 = 3
So 869210-33-3 is a valid CAS Registry Number.

869210-33-3Downstream Products

869210-33-3Relevant academic research and scientific papers

Asymmetric synthesis of 4′-quaternary 2′-deoxy-3′-epi- β-C-nucleosides

Enders, Dieter,Hieronymi, Antje,Ridder, André

, p. 2391 - 2393 (2005)

An efficient diastereo- and enantioselective synthesis of 4′-quaternary 2′-deoxy-3′-epi-β-C-nucleosides is described employing the RAMP-hydrazone methodology to establish the first stereocentre. Further key steps include diastereoselective nucleophilic 1,

Asymmetric synthesis of 4′-quaternary 2′-deoxy-3′- and -4′-epi-β-C- and -N-nucleosides

Enders, Dieter,Hieronymi, Antje,Raabe, Gerhard

experimental part, p. 1545 - 1558 (2009/04/03)

A versatile and efficient route to both enantiomers of 4′-quaternary 2′-deoxy-3′- and -4′-epi-β-C- and -N-nucleosides is described. The asymmetric synthesis involves the SAMP/RAMP-hydrazone α-alkylation methodology and diastereoselective nucleophilic 1,2-

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