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5′-O-(4,4′-dimethoxytrityl)-3′-O-[2-cyanoethoxy-(N,N-diisopropylamino)-phosphino]-5-vinyl-2′-deoxyuridine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

287980-24-9

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287980-24-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 287980-24-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,8,7,9,8 and 0 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 287980-24:
(8*2)+(7*8)+(6*7)+(5*9)+(4*8)+(3*0)+(2*2)+(1*4)=199
199 % 10 = 9
So 287980-24-9 is a valid CAS Registry Number.

287980-24-9Downstream Products

287980-24-9Relevant academic research and scientific papers

Template-directed reversible photocircularization of DNA via 5-vinyldeoxycytidine

Fujimoto,Matsuda,Ogawa,Hayashi,Saito

, p. 6451 - 6454 (2000)

An efficient and reversible template-directed photoligation of oligodeoxynucleotides (ODNs) using 5-vinyldeoxycytidine ((v)c) was described. When ODN containing (v)C at the 5' end was photoirradiated with ODN containing thymine at the 3' end in the presence of a template ODN, an efficient photoligation was observed. Reversible photopadlocking of a circular DNA by the photocircularization using (v)C was demonstrated. (C) 2000 Elsevier Science Ltd.

Chemoselective Modification of Vinyl DNA by Triazolinediones

Naik, Anu,Alzeer, Jawad,Triemer, Therese,Bujalska, Anna,Luedtke, Nathan W.

supporting information, p. 10850 - 10853 (2017/08/30)

A new method for the post-synthetic modification of nucleic acids was developed that involves mixing a phenyl triazolinedione (PTAD) derivative with DNA containing a vinyl nucleobase. The resulting reactions proceeded through step-wise mechanisms, giving either a formal [4+2] cycloaddition product, or, depending on the context of nucleobase, PTAD addition along with solvent trapping to give a secondary alcohol in water. Catalyst-free addition between PTAD and the terminal alkene of 5-vinyl-2′-deoxyuridine (VdU) was exceptionally fast, with a second-order rate constant of 2×103 m?1 s?1. PTAD derivatives selectively reacted with VdU-containing oligonucleotides in a conformation-selective manner, with higher yields observed for G-quadruplex versus duplex DNA. These results demonstrate a new strategy for copper-free bioconjugation of DNA that can potentially be used to probe nucleic acid conformations in cells.

Detection of methylcytosine by DNA photoligation via hydrophobic interaction of the alkyl group

Ogino, Masayuki,Taya, Yuuta,Fujimoto, Kenzo

supporting information; experimental part, p. 3163 - 3167 (2011/02/25)

We report the nonenzymatic detection of 5-methylcytosine by using template-directed photoligation through 5-vinyl-2′-deoxyuridine derivatives with high selectivity. In this paper, we propose a new detection method by using hydrophobic interaction. The photoligation yield of the 5-methylcytosine case was approximately 5.6-fold higher than that in the case of cytosine.

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