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S,S-diphenyl thymidine 3'-phosphorodithioate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

70900-95-7

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70900-95-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 70900-95-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,9,0 and 0 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 70900-95:
(7*7)+(6*0)+(5*9)+(4*0)+(3*0)+(2*9)+(1*5)=117
117 % 10 = 7
So 70900-95-7 is a valid CAS Registry Number.

70900-95-7Relevant academic research and scientific papers

OLIGODEOXYRIBONUCLEOTIDE SYNTHESIS BY USE OF S,S-DIPHENYL DEOXYRIBONUCLEOSIDE 3'-PHOSPHORODITHIOATES AND BIFUNCTIONAL CONDENSING REAGENTS IN THE PHOSPHOTRIESTER APPROACH

Sekine, Mitsuo,Matsuzaki, Jun-Ichi,Hata, Tsujiaki

, p. 5279 - 5288 (2007/10/02)

Four kinds of arenedisulphonyl chlorides as condensing reagents for oligodeoxyribonucleotide synthesis have been synthesised and their condensing abilities were examined in the synthesis of thymidylyl(3'-5')thymidine.Among them, mesitylenedisulphonyl chlo

4,4',4''-Tris(levulinoyloxy)trityl as a New Type of Primary Hydroxyl Protecting Group

Sekine, Mitsuo,Hata, Tsujiaki

, p. 336 - 339 (2007/10/02)

The 4,4',4''-tris(levulinoxy)trityl (TLTr) group was introduced selectively on the 5'-oxygen of thymidine by use of in situ generated 4,4',4''-tris(levulinoyloxy)trityl bromide.The TLTr group was found to be sufficiently stable to acids and readily removed by hydrazinolysis followed by warming to 50 deg C in pyridine-acetic acid without damage of other protecting groups such as the O-acetyl and 4,4'-dimethoxytrityl groups.The utility of this new protecting group was demonstrated by the successful synthesis of thymidylyl(3'-5')thymidine where the TLTr group was employed as 5'-hydroxyl-protecting group.

Cyclic Orthoester Functions as New Protecting Groups in Nucleosides

Sekine, Mitsuo,Hata, Tsujiaki

, p. 2044 - 2049 (2007/10/02)

Four kinds of cyclic orthoester functions have been studied as protecting groups of hydroxyl groups in nucleosides.Among them, the 1,3-benzodithiol-2-yl (BDT) group was found to have several promising properties.This group can be easily introduced into nu

PHOSPHOTRIESTER APPROACH TO OLIGOTHYMIDYLATE SYNTHESIS UTILIZING A SIMPLE THYMIDINE UNIT AND A NEW TYPE OF CONDENSING AGENT

Sekine, Mitsuo,Matsuzaki, Jun-ichi,Hata, Tsujiaki

, p. 3209 - 3212 (2007/10/02)

DMTrTp(SPh)2 was proposed as a simplest "nucleotide unit" for the synthesis of olygothymidylates.One phenylthio group was removed selectively and rapidly from dithiol-esters by 1M pyridinium hypophosphonate.Two kinds of arenedisulfonyl chlorides were newl

Synthesis and Properties of S,S-Diaryl Thymidine Phosphorodithioates

Sekine, Mitsuo,Hamaoki, Ken,Hata, Tsujiaki

, p. 3815 - 3827 (2007/10/02)

Appropriately protected and unprotected S,S-diphenyl thymidine 3'- or 5'-phosphorodithioates and S,S-bis(4-methoxyphenyl) thymidine 3'- or 5'-phosphorodithioates were successfully prepared by the reaction of the thymidine derivatives with cyclohexylammoni

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