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2'-deoxy-2'-difluoromethylene-5'-dimethoxytrityluridine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

170112-35-3

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170112-35-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 170112-35-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,0,1,1 and 2 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 170112-35:
(8*1)+(7*7)+(6*0)+(5*1)+(4*1)+(3*2)+(2*3)+(1*5)=83
83 % 10 = 3
So 170112-35-3 is a valid CAS Registry Number.

170112-35-3Relevant academic research and scientific papers

Synthesis and NMR spectra of some new carbohydrate modified uridine phosphoramidites

Serafinowski, Pawel J.,Barnes, Colin L.

, p. 1529 - 1532 (2007/10/03)

The one step reaction of 2'- and 3'-keto derivatives of uridine with bromodifluoromethyl[tris(dimethylamino)]phosphonium bromide and zinc gives the corresponding 2'- and 3'-difluoromethylene nucleosides in good yield. Desilylation and phosphitylation of the resultant 2'- or 3'-hydroxyls provides the target 2'- and 3'-phosphoramidites 7 and 8 for use in oligonucleotide synthesis.

New method for the preparation of 3'- and 2'-phosphoramidites of 2'- and 3'-difluoromethyleneuridine

Serafinowski,Barnes

, p. 7929 - 7938 (2007/10/03)

The one step reaction of 2'- and 3'-keto derivatives of uridine 2a, 2b, 7a and 7b with bromodifluoromethyl[tris(dimethylamino)]phosphonium bromide (13) and zinc gives the corresponding 2'- and 3'-difluoromethylene nucleosides 3a, 3b, 8a and 8b in good yield. Removal of the silyl groups affords difluoromethylenated uridines 4a, 4b, 9a and 9b. Phosphitylation of 4a and 9a provides the target 2'- and 3'-phosphoramidites 5 and 10 for use in oligonucleotide synthesis.

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