CAS 163878-63-5
:Uridina,5'-O-[bis(4-metossifenile)fenilmetile]-2'-O-(2-metossietile)-5-metile-, 3'-[2-cianoetile bis(1-metiletile)fosforamidite]
- 5-Methyl-5'-DMT-2'-O-Methyl-Uridine
- DMT-2'-O-MOE-T-CE Phosphoramidite
- 5-Me-DMT-2'-O-MOE-U-CE-Phosphoramidite
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DMT-2'-O-MOE-5-Me-rU Phosphoramidite
CAS:Formula:C43H55N4O10PPurezza:>95.0%(HPLC)Colore e forma:White to Light yellow powder to crystalPeso molecolare:818.902'-MOE T β-Cyanoethyl Phosphoramidite
CAS:Nucleic acids and their salts, whether or not chemically defined; other heterocyclic compounds, nesoiFormula:C43H55N4O10PColore e forma:White Off-White Pale Yellow PowderPeso molecolare:818.365582'-O-Moe-5Meu-3'-Phosphoramidite
CAS:2'-O-Moe-5Meu-3'-PhosphoramiditeFormula:C43H55N4O10PPurezza:97%Peso molecolare:818.892'-O-MOE-5MeU-3'-phosphoramidite
CAS:2'-O-MOE-5MeU-3'-phosphoramidite is a Nucleoside Phosphoramidite.Formula:C43H55N4O10PColore e forma:SolidPeso molecolare:818.89DMT-2′O-MOE-rMeU Phosphoramidite (5-Me-U-2'-MOE-Phosphoramidite)
CAS:Formula:C43H55N4O10PPurezza:98%Colore e forma:SolidPeso molecolare:818.8914DMT-2′O-MOE-rMeU Phosphoramidite
CAS:(2R,3R,4R,5R)-2-((Bis(4-methoxyphenyl)(phenyl)methoxy)methyl)-4-(2-methoxyethoxy)-5-(5-methyl-2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)tetrahydrofuran-3-yl (2-cyanoethyl) diisopropylphosphoramiditeFormula:C43H55N4O10PPurezza:95%Peso molecolare:818.895'-O-DMT-2'-O-(2-methoxyethyl)-5-methyluridine 3'-CE phosphoramidite
CAS:5'-O-DMT-2'-O-(2-methoxyethyl)-5-methyluridine 3'-CE phosphoramidite is a nucleoside phosphoramidite used as a building block for the introduction of uridine units into oligonucleotides. 5'-O-DMT-2'-O-(2-methoxyethyl)-5-methyluridine 3'-CE phosphoramidite is used for a broad range of applications including the synthesis of natural and unnatural DNA and RNA strands. Phosphoramidites are the reagent class of choice for oligonucleotide synthesis as they contain readily removable orthogonal protecting groups and can be produced at reasonable scales. The diisopropylamino leaving group is readily cleaved upon exposure to an azole catalyst allowing for a highly efficient coupling reaction with a free hydroxyl group on the growing oligonucleotide and oxidation of the subsequent phosphite triester, followed by beta-elimination of the cyanoethyl group affords the stable phosphodiester linkage.
Formula:C43H55N4O10PPurezza:Min. 95%Colore e forma:White PowderPeso molecolare:818.89 g/mol








