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2-nitrobenzyl 3-O-(2-cyanoethyl)-N,N-diisopropylphosphoramidyl-4-methoxy-5-O-(4,4'-dimethoxytrityl)-2-deoxy-D-ribofuranoside is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1005174-08-2

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1005174-08-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1005174-08-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,0,5,1,7 and 4 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1005174-08:
(9*1)+(8*0)+(7*0)+(6*5)+(5*1)+(4*7)+(3*4)+(2*0)+(1*8)=92
92 % 10 = 2
So 1005174-08-2 is a valid CAS Registry Number.

1005174-08-2Downstream Products

1005174-08-2Relevant academic research and scientific papers

Photochemical generation of oligodeoxynucleotide containing a C4′-oxidized abasie site and its efficient amine modification: Dependence on structure and microenvironment

Usui, Kazuteru,Aso, Mariko,Fukuda, Mitsuhiro,Suemune, Hiroshi

, p. 241 - 248 (2008/09/19)

(Chemical Equation Presented) Bleomycin-induced oxidative DNA damage under limited oxygen conditions results in the formation of the C4′-oxidized abasic site (1). We synthesized the oligodeoxynucleotides (ODN) 5, which contains 4′-o-nitrobenzyloxythymidine (3), and 6, which contains 2-nitrobenzyloxy-4′-methoxy-2′-deoxy-D-ribofuranoside (4) as the caged precursors of 7, an ODN containing 1, to study its reactivity with amines Photoirradiation of the single- and double-stranded 5 led to the formation of 7. Uncaging of the duplex was faster and the yield of 7 was higher with the double-stranded than with the single-stranded ODN. It was suggested that a low dielectric environment of the o-nitrobenzyloxy group in the minor groove of the duplex might accelerate the uncaging rate. Similarly, 6 and its duplex yielded 7 by photoirradiation However, the yields of 7 were lower than those of 5, and duplex formation slowed the uncaging rate. Reaction of the obtained 7 with an amine resulted in the formation of the lactam 2b in good yield in both single- and double-stranded forms, showing that amine modification of biomolecules by an ODN containing 1 is possible under physiologic conditions.

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