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5-(3-trifluoroacetamidopropargyl)-5'-O-(4,4'-dimethoxytrityl)-2'-deoxyuridine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

120016-97-9

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120016-97-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 120016-97-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,0,0,1 and 6 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 120016-97:
(8*1)+(7*2)+(6*0)+(5*0)+(4*1)+(3*6)+(2*9)+(1*7)=69
69 % 10 = 9
So 120016-97-9 is a valid CAS Registry Number.

120016-97-9Relevant academic research and scientific papers

OLIGONUCLEOTIDE LABELLING: A CONCISE SYNTHESIS OF A MODIFIED THYMIDINE PHOSPHORAMIDITE

Cruickshank, Kenneth A.,Stockwell, Daniel L.

, p. 5221 - 5224 (1988)

The condensation of 5'-dimethoxytrityl-5-iodo-2'-deoxyuridine (1) with N-trifluoroacetylpropargylamine (2) in the presence bis(triphenylphosphine) Pd(II) chloride and copper(I) iodide and subsequent conversion to the 3'-phosphoramidite (4) is an efficient

A rapidly photo-activatable light-up fluorescent nucleoside and its application in DNA base variation sensing

He, Zhiyong,Chen, Yuqi,Wang, Yafen,Wang, Jiaqi,Mo, Jing,Fu, Boshi,Wang, Zijing,Du, Yuhao,Zhou, Xiang

, p. 8545 - 8548 (2016)

A new DNA building block (dTetU) bearing a tetrazole and allyloxy group at N-phenyl ring linked through an aminopropynyl linker to the 5-position of 2′-deoxyuridine was synthesized. The modified DNA can be lit up via a photoinduced intramolecul

Functionalization of mono- and oligonucleotides with phosphane ligands by amide bond formation

Nuzzolo, Marzia,Grabulosa, Arnald,Slawin, Alexandra M. Z.,Meeuwenoord, Nico J.,Van Der Marel, Gijsbert A.,Kamer, Paul C. J.

scheme or table, p. 3229 - 3236 (2010/08/20)

Seven phosphane-functionalized deoxyuridines have been prepared by amide bond formation between aminodeoxyuridines and phosphanylcarboxylic acids. X-ray crystal structures for two of these new modified nucleosides have been obtained. The same coupling method has been extended to oligonucleotides. The phosphane containing strands have been purified and characterized by MALDI-TOF and, for the first time, 31P NMR spectrometry. Coordination of a phosphane-modified 15-mer to a [PdCl(η3-allyl)] moiety has been confirmed by 31P NMR spectroscopy.

STABILIZED NUCLEIC ACID DARK QUENCHER-FLUOROPHORE PROBES

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Page/Page column 29, (2009/10/21)

The present invention provides a new class of solids supports for synthesis of modified oligomers of nucleic acids, and nucleic acid probes that have a format expediently synthesized on the new supports. Exemplary solid supports include at least one quenc

Building-block approach for the straightforward incorporation of a new FRET (fluorescence-resonance-energy transfer) system into synthetic DNA

Clima, Lilia,Bannwarth, Willi

, p. 165 - 175 (2008/09/17)

The synthesis of the two new phosphoramidites 5 and 8 bearing a carbostyril (= quinolin-2(1H)-one) chromophore used as donor entity in our recently developed new FRET (fluorescence-resonance-energy transfer) system is described (Schemes 1 and 2) The high

DNA minicircles with gaps for versatile functionalization

Rasched, Goran,Ackermann, Damian,Schmidt, Thorsten L.,Broekmann, Peter,Heckel, Alexander,Famulok, Michael

, p. 967 - 970 (2008/09/20)

(Figure Presented) Doing the rounds: A highly straightforward approach has been developed that provides access to DNA minicircles containing a 21-mer single-stranded gap region of defined sequence (see picture). The single-stranded domain within a small c

Application of a highly robust and efficient fluorescence-resonance-energy- transfer (FRET) system in DNA

Clima, Lilia,Hirtz-Haag, Caroline,Kienzler, Andrea,Bannwarth, Willi

, p. 1082 - 1098 (2008/03/12)

We report a feasibility study for the application of our newly developed highly efficient and robust fluorescence-resonance-energy-transfer (FRET) system to DNA. A 2′-oligodeoxynucleotide, 12, equipped with a quinolinone derivative as donor and a (bathoph

Quantitative analysis of receptors for adenosine nucleotides obtained via in vitro selection from a library incorporating a cationic nucleotide analog

Battersby, Thomas R.,Ang, Darwin N.,Burgstaller, Petra,Jurczyk, Simona C.,Bowser, Michael T.,Buchanan, Danielle D.,Kennedy, Robert T.,Benner, Steven A.

, p. 9781 - 9789 (2007/10/03)

5-(3″-Aminopropynyl)-2′-deoxyuridine (dJ), a modified nucleoside with a side chain carrying a cationic functional group, was incorporated into an oligonucleotide library, which was amplified using the Vent DNA polymerase in a polymerase chain reaction (PC

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