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3'-(Trityl)amino-5'-O-(tert-butyldimethylsilyl)-2',3'-dideoxycytidine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

195375-45-2

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195375-45-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 195375-45-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,5,3,7 and 5 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 195375-45:
(8*1)+(7*9)+(6*5)+(5*3)+(4*7)+(3*5)+(2*4)+(1*5)=172
172 % 10 = 2
So 195375-45-2 is a valid CAS Registry Number.

195375-45-2Relevant academic research and scientific papers

Synthons for synthesis of oligonucleotide N3-P5 phosphoramidates

-

, (2008/06/13)

The invention provides a method of synthesizing oligonucleotide N3'→P5' phosphoramidates using an amine-exchange reaction of phosphoramidites in which a -deprotected 3'-amino group of a solid phase supported oligonucleotide chain is exhanged for the amino

Solid phase synthesis of oligonucleotide N3'-P5' phosphoramidates

-

, (2008/06/13)

The invention provides a method of synthesizing oligonucleotide N3'→P5' phosphoramidates using an amine-exchange reaction of phosphoramidites in which a deprotected 3'-amino group of a solid phase supported oligonucleotide chain is exhanged for the amino

N3′→P5′ Oligodeoxyribonucleotide Phosphoramidates: A New Method of Synthesis Based on a Phosphoramidite Amine-Exchange Reaction

Nelson, Jeffrey S.,Fearon, Karen L.,Nguyen, Mark Q.,McCurdy, Sarah N.,Frediani, Jeff E.,Foy, Michael F.,Hirschbein, Bernard L.

, p. 7278 - 7287 (2007/10/03)

A new method for the synthesis of N3′→P5′ phosphoramidate oligodeoxynucleotides is demonstrated. Described herein is the synthesis of the monomers utilized in the phosphoramidite amine-exchange process and the experimental details pertaining to this new mode of chain assembly. The phosphoramidite amine-exchange method generates coupling yields in the 92-95% range per cycle and further enables the synthesis of chimeric phosphoramidate/phosphodiester or phosphoramidate/ phosphorothioate oligonucleotides with no instrument modifications.

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