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9-{(4aR,7S,8S,8aS)-8-[(4-Methoxy-phenyl)-diphenyl-methoxymethyl]-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-7-yl}-9H-purin-6-ylamine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

203383-44-2

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203383-44-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 203383-44-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,3,3,8 and 3 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 203383-44:
(8*2)+(7*0)+(6*3)+(5*3)+(4*8)+(3*3)+(2*4)+(1*4)=102
102 % 10 = 2
So 203383-44-2 is a valid CAS Registry Number.

203383-44-2Downstream Products

203383-44-2Relevant academic research and scientific papers

Facile synthesis of 3'-C-branched 1,5-anhydrohexitol nucleosides

Hossain, Nafizal,Herdewijn, Piet

, p. 1781 - 1786 (2007/10/03)

The 3'-β-C-branched anhydrohexitol nucleosides have been conveniently synthesised starting from commercially available D-ribose following the reaction sequence: (i) conversion of protected pentofuranose sugar to the corresponding hexopyranosyl nitrosugar (ii) addition of the conjugate base of nitrosugar to formaldehyde to obtain C-branched nitro sugar (iii) removal of nitro group by n-tributyltin hydride treatment and (iv) Mitsunobu type alkylation to build up the nucleobase.

Synthesis of 3'-C-branched 1',5'-anhydromannitol nucleosides as new antiherpes agents

Hossain, Nafizal,Van Halbeek, Herman,De Clercq, Erik,Herdewijn, Piet

, p. 2209 - 2226 (2007/10/03)

A series of 3'-β-C-branched anhydromannitol nucleosides were conveniently synthesized starting from commercially available D-ribose. The reaction sequences were: (i) conversion of the protected pentofluranose to the corresponding nitrohexopyranose; (ii) addition of the conjugated base of the nitrosugar to formaldehyde; (iii) removal of the nitro group by n-tributyltin hydride treatment and (iv) Mitsunobu type alkylation to introduce the nucleobase. The conformation of intermediates and final compounds were deduced from NMR analysis. The thymine congener showed potent activity against herpes simplex virus (HSV).

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