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Phosphoric acid (2R,3R,4R,5R)-5-[bis-(4-methoxy-phenyl)-phenyl-methoxymethyl]-4-(tert-butyl-dimethyl-silanyloxy)-2-(2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-tetrahydro-furan-3-yl ester 2-chloro-phenyl ester; compound with triethyl-amine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

134009-25-9

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134009-25-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 134009-25-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,4,0,0 and 9 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 134009-25:
(8*1)+(7*3)+(6*4)+(5*0)+(4*0)+(3*9)+(2*2)+(1*5)=89
89 % 10 = 9
So 134009-25-9 is a valid CAS Registry Number.

134009-25-9Downstream Products

134009-25-9Relevant academic research and scientific papers

Design, synthesis and systematic evaluation of all possible cyclic dinucleotides (CDNs) that activate human stimulator of interferon genes (STING) variants

Li, Lu-Yuan,Ma, De-Jun,Wang, Chuan-Lin,Wang, Da-Wei,Wang, Zheng-Hua,Wen, Xin,Xi, Zhen,Zhang, Hang,Zhang, Qiang-Zhe,Zhao, Can-Can

, (2020/04/10)

Cyclic dinucleotides (CDNs) are known to activate stimulator of interferon genes (STING) and induce type I interferon responses, therefor possess great potentials to be of immunotherapeutic value for cancers and infectious diseases. However, the existence

Spectroscopic and enzymatic chracterization of 2'-5' and 3'-5' RNA hexamers AACCUU synthesised by phosphotriester approach in solution using 2'-t-butyldimethylsilyl protection

Gopalakrishnan,Ganesh,Gunjal,Likhite

, p. 1075 - 1090 (2007/10/02)

Comparative 1H, 31P NMR and CD spectroscopic results and enzymatic cleavage of single stranded RNA hexamers which have identical base sequence (AACCUU) but are regioisomeric at the internucleotide phosphate linkages (2'-5', 3'-5' and their covalent hybrid) are presented. The 31P NMR results revealed significant differences in local phosphate backbone conformation among these isomers, with 2'-5' isomer exhibitingf maximum heterogeneity as compared to the 3'-5' isomer, the analogous DNA hexamer and the covalent hybrid hexamer. In contrast to this, there are no appreciable differences in the overall base-base stacking as seen in the CD spectra of 2'-5' and 3'-5' isomers. All RNA hexamers were synthesised by solution phase phosphotriester chemistry with t-butyldimethylsilyl (TBDMS) as 2'-O-protecting group. The fully protected oligorobomers were deprotected in two steps: (i) saturated anhydrous MeOH-NH3 for phosphate and amino deprotections and (ii) TBAF for removal of 2'-O-TBDMS group. Use of sat. MeOH-NH3 (instead of aq. NH3) prevents 2'-3' internucleotide phosphate migrations, chain fragmentations and 5'-terminal modifications by neighbouring group participation (NGP). The retention of isomeric integrity and absence of 5'-terminal modification in the final products was established by digestion with several nucleases.

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