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Diisopropyl-phosphoramidous acid (2R,3S,5R)-2-[bis-(4-methoxy-phenyl)-phenyl-methoxymethyl]-5-(2,4-dioxo-5-phenylsulfanylmethyl-3,4-dihydro-2H-pyrimidin-1-yl)-tetrahydro-furan-3-yl ester 2-cyano-ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

272116-47-9

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272116-47-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 272116-47-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,7,2,1,1 and 6 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 272116-47:
(8*2)+(7*7)+(6*2)+(5*1)+(4*1)+(3*6)+(2*4)+(1*7)=119
119 % 10 = 9
So 272116-47-9 is a valid CAS Registry Number.

272116-47-9Relevant academic research and scientific papers

Independent Generation of 5-(2′-Deoxycytidinyl)methyl Radical and the Formation of a Novel Cross-Link Lesion between 5-Methylcytosine and Guanine

Zhang, Qibin,Wang, Yinsheng

, p. 12795 - 12802 (2007/10/03)

Reactive oxygen species (ROS) can damage DNA. Although a number of single nucleobase lesions induced by ROS have been structurally characterized, only a few intrastrand cross-link lesions have been identified and characterized, and all of them involve adj

Synthesis and UV photolysis of oligodeoxynucleotides that contain 5-(phenylthiomethyl)-2'-deoxyuridine: a specific photolabile precursor of 5-(2'-deoxyuridilyl)methyl radical.

Romieu,Bellon,Gasparutto,Cadet

, p. 1085 - 1088 (2007/10/03)

[formula: see text] The title exocyclic radical (2) is generated via photochemical cleavage of 5-(phenylthiomethyl)-2'-deoxyuridine (8). The latter thionucleoside (8) was successfully incorporated into DNA oligomers by automated DNA synthesis using phosphoramidite chemistry. UV exposure of 8 containing oligonucleotides under (an)aerobic conditions gives rise to specific base lesions. The photoproducts have been isolated and further characterized on the basis of detailed NMR and mass spectrometric analyses.

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