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225108-20-3

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225108-20-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 225108-20-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,5,1,0 and 8 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 225108-20:
(8*2)+(7*2)+(6*5)+(5*1)+(4*0)+(3*8)+(2*2)+(1*0)=93
93 % 10 = 3
So 225108-20-3 is a valid CAS Registry Number.

225108-20-3Relevant articles and documents

Silylation-mediated transesterification of O-phenyl H-phosphonothioates - A new entry to nucleoside H-phosphonothioate monoesters

Laven, Gaston,Nilsson, Johan,Stawinski, Jacek

, p. 5111 - 5114 (2007/10/03)

O-Phenyl H-phosphonothioate undergoes a facile transesterification with suitably protected nucleosides upon in situ silylation with tert- butyldiphenylsilyl chloride in pyridine/toluene to produce the corresponding 3′-H-phosphonothioates in good yields. Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2004.

Aryl H-Phosphonates. 12. Synthetic and 31P NMR Studies on the Preparation of Nucleoside H-Phosphonothioate and Nucleoside H-Phosphonodithioate Monoesters

Cieslak, Jacek,Jankowska, Jadwiga,Stawinski, Jacek,Kraszewski, Adam

, p. 7049 - 7054 (2007/10/03)

Transformation of nucleoside H-phosphonate monoesters into the corresponding H-phosphonothioate and H-phosphonodithioate derivatives and possible side-reactions that may accompany this process were studied using 31P NMR spectroscopy. These provided new insight into a possible mechanism involved in this transformation and constituted the basis for development of efficient methods for the preparation of nucleoside H-phosphonothioate and nucleoside H-phosphonodithioate monoesters using readily available H-phosphonate monoesters as starting materials.

NUCLEOSIDE H-PHOSPHONATES. X. STUDIES ON NUCLEOSIDE HYDROGENPHOSPHONOTHIOATE DIESTER SYNTHESIS

Stawinski, Jacek,Thelin, Mats,Zain, Rula

, p. 2157 - 2160 (2007/10/02)

Synthesis and chemical properties of nucleoside H-phosphonothioates are discussed in the context of possible application of these compounds as intermediates in the synthesis of oligonucleotide analogues.

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