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3,5-di-O-benzyl-4-C-(hydroxymethyl)-1,2-di-O-isopropylidene-3-C-vinyl-α-D-ribofuranose is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

879546-88-0

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879546-88-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 879546-88-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,9,5,4 and 6 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 879546-88:
(8*8)+(7*7)+(6*9)+(5*5)+(4*4)+(3*6)+(2*8)+(1*8)=250
250 % 10 = 0
So 879546-88-0 is a valid CAS Registry Number.

879546-88-0Downstream Products

879546-88-0Relevant academic research and scientific papers

Synthesis of the 3′-C-hydroxymethyl-branched locked nucleic acid thymidine monomer

Kumar, Surender,Sharma, Pawan K.,Stein, Paul C.,Nielsen, Poul

experimental part, p. 5715 - 5722 (2009/06/08)

A 3′-C-hydroxymethyl-branched Locked Nucleic Acid (LNA) monomer 3 was synthesized from diacetone-α-D-glucose taking advantage of a stereoselective Grignard reaction for the introduction of a vinyl group, an aldol/Cannizzarro sequence for introducing the 4

Synthesis of a branched locked nucleic acid (LNA) analogue

Sharma, Pawan K.,Kumar, Surender,Nielsen, Poul

, p. 1505 - 1508 (2008/09/18)

A 3′-C-branched LNA-type bicyclic nucleoside, containing a furanose ring locked in an N-type conformation, was synthesized from a known 3-C-vinyl allofuranose derivative using a strategy relying on the condensation with the nucleobase after the introducti

Synthesis and properties of trans-3′,4′-bridged nucleic acids having typical S-type sugar conformation

Sekiguchi, Mitsuaki,Obika, Satoshi,Harada, Yasuki,Osaki, Tomohisa,Somjing, Roongjang,Mitsuoka, Yasunori,Shibata, Nao,Masaki, Miyuki,Imanishi, Takeshi

, p. 1306 - 1316 (2007/10/03)

The synthesis of nucleoside analogues with a conformationally restricted sugar moiety is of great interest. The present research describes the synthesis of BNA (bridged nucleic acid) monomers 1 and 2 bearing a 4,7-dioxabicyclo[4.3.0] nonane skeleton and a methoxy group at the C2' position. Conformational analysis showed that the sugar moiety of these monomers is restricted in a typical S-type conformation. It was difficult to synthesize the phosphoramidite derivative of the ribo-type monomer 1, while the phosphoramidite of the arabino-type monomer 2 was successfully prepared and incorporated into oligodeoxynucleotides (ODNs). The hybridization ability of the obtained ODN derivatives containing 2 with complementary strands was evaluated by melting temperature (Tm) measurements. As a result, the ODN derivatives hybridized with DNA and RNA complements in a sequence-selective manner, though the stability of the duplexes was lower than that of the corresponding natural DNA/DNA or DNA/RNA duplex.

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