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4-N-benzoyl-2-C-β-methylcytidine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

220503-82-2

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220503-82-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 220503-82-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,0,5,0 and 3 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 220503-82:
(8*2)+(7*2)+(6*0)+(5*5)+(4*0)+(3*3)+(2*8)+(1*2)=82
82 % 10 = 2
So 220503-82-2 is a valid CAS Registry Number.

220503-82-2Relevant academic research and scientific papers

2'-C-branched ribonucleosides: Synthesis of the phosphoramidite derivatives of 2'-C-β-methylcytidine and their incorporation into oligonucleotides

Tang, Xiao-Qing,Liao, Xiangmin,Piccirilli, Joseph A.

, p. 747 - 754 (1999)

We describe a strategy for the incorporation of a 2'-C-branched ribonucleoside, 2'-C-β-methylcytidine, into oligonucleotides via solid- phase synthesis using phosphoramidite derivatives. 4-N-Benzoyl-2'-C-β- methylcytidine (2b) was synthesized by coupling persilylated 4-N- benzoylcytosine with 1,2,3,5-tetra-O-benzoyl-2-C-β-methyl-α-(and β)-D- ribofuranose (1) in the presence of SnCl4 in acetonitrile, followed by selective deprotection with NaOH in pyridine/methanol. The 3'- and 5'- hydroxyl groups were blocked as a cyclic di-tert-butylsilanediyl ether 3 by treatment with di-tert-butyldichlorosilane/AgNO3 in DMF. The 2'-hydroxyl group was then protected as a tert-butyldimethylsilyl ether 4a by treatment with tert-butylmagnesium chloride followed by addition of tert- butyldimethylsilyl trifluoromethanesulfonate in THF. As an alternative to 2'- silyl protection, the corresponding 2'O-tetrahydropyranyl ether 4b was prepared by treatment of 3 with 4,5-dihydro-2H-pyran in the presence of a catalytic amount of 10-camphorsulfonic acid in methylene chloride. The di- tert-butylsilanediyl groups of 4a and 4b were removed by treatment with pyridinium poly(hydrogen fluoride) to afford 5a and 5b, respectively. Protection of the 5'-hydroxyl group as a dimethoxytrityl ether and phosphitylation of the 3'-hydroxyl group by the standard procedure gave the phosphoramidite derivatives 7a and 7b. Both 7a and 7b could be used to incorporate 2'-C-β-methylcytidine into oligonucleotides efficiently via standard solid-phase synthesis, but the tetrahydropyranyl group of 7b was more readily removed from oligonucleotides than the tert-butyldimethylsilyl group of 7a. Oligonucleotides containing 2'-C-β-methylcytidine undergo base- catalyzed degradation analogous to natural RNA.

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