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Thymidine, 5'-O-[(1,1-dimethylethyl)diphenylsilyl]-, 3'-(O-phenyl carbonothioate) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

161085-74-1

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161085-74-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 161085-74-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,1,0,8 and 5 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 161085-74:
(8*1)+(7*6)+(6*1)+(5*0)+(4*8)+(3*5)+(2*7)+(1*4)=121
121 % 10 = 1
So 161085-74-1 is a valid CAS Registry Number.

161085-74-1Relevant academic research and scientific papers

Efficient and stereoselective synthesis of 3'-deoxy 3'-C-branched-chain substituted thymidine

Sanghvi,Bharadwaj,Debart,De Mesmaeker

, p. 1163 - 1166 (1994)

In this report, we provide for the first time a facile, efficient, and stereoselective synthesis of 1-[5-O-(tert-butyldiphenylsilyl)-2,3-dideoxy-3-C-formyl-β-D-erythro-p entofuranosyl]thymine (12), using an intermolecular radical C-C bond formation reacti

Synthesis of 3′-C-substituted thymidine derivatives by free-radical techniques: scope and limitations

Horton, Derek,Chen, Kuangmin,No, Zaesung,Lee, Howard C.

, p. 259 - 267 (2007/10/03)

The scope and limitations of radical-mediated 3′-C-substitution of pyrimidine nucleosides was evaluated with 5′-O-(tert-butyldimethylsilyl)thymidine or its tert-butyldiphenylsilyl analogue having thionoester or thionoamide groups at O-3′, including (methy

Nucleoside homodimerisation by cross metathesis

Batoux, Nathalie,Benhaddou-Zerrouki, Rachida,Bressolier, Philippe,Granet, Robert,Laumont, Géraldine,Aubertin, Anne-Marie,Krausz, Pierre

, p. 1491 - 1493 (2007/10/03)

The cross metathesis of 3′-allylic analogues of thymidine, 2′-deoxyuridine and 2′-deoxycytidine is used to obtain nucleoside dimers, in which an unsaturated hydrocarbon chain links the 3′ positions of the sugar moieties. The biological activity on HIV inf

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