This compound is a modified phosphoramidite reagent specifically designed for DNA oligonucleotide synthesis. Its structure incorporates a cEt (constrained ethyl) modification and a dimethoxytrityl (DMT) protecting group, which are important for stabilizing oligonucleotides and enabling efficient solid-phase synthesis.
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CAS 1197033-19-4
(1R,3R,4R,7S)-3-(6-N-Benzoyladenin-9-yl)-7-(2-cyanoethoxy(diisopropylamino)phosphinoxy)-1-(4,4'-dimethoxytrityloxymethyl)-2,5-dioxabicyclo(2.2.1)heptane
phosphoramidite building block for oligonucleotide synthesis
5'-ODMT cEt N-Bzm5 C Phosphoramidite (Amidite)
Modified nucleoside phosphoramidite for oligonucleotide synthesis
9-(2,5-Anhydro-4-((bis(4-methoxyphenyl)(phenyl)methoxy)methyl)-3-O-((2-cyanoethoxy)(di(propan-2-yl)amino)phosphanyl)-6-deoxy-alpha-L-mannofuranosyl)-2-(2-methylpropanamido)-3,9-dihydro-6H-purin-6-one
Phosphoramidite for oligonucleotide synthesis
(2-((2,5-Dichloropyrimidin-4-yl)amino)phenyl)dimethylphosphine oxide
research compound
1,2,4,5-Tetrachlorobenzene-d2
deuterated research standard
1,3,5-Trichlorobenzene-d3
Deuterated analytical reference standard
4-Phenyl-2-pyrrolidinone
Research compound for organic synthesis
N-(9-((1R,3R,4R,7S)-1-((bis(4-methoxyphenyl)(phenyl)methoxy)methyl)-7-hydroxy-2,5-dioxabicyclo[2.2.1]heptan-3-yl)-9H-purin-6-yl)benzamide
modified nucleoside intermediate for oligonucleotide synthesis
N-[9-[(1S,3R,4R,6S,7S)-1-[[bis(4-methoxyphenyl)-phenylmethoxy]methyl]-7-[2-cyanoethoxy-[di(propan-2-yl)amino]phosphanyl]oxy-6-methyl-2,5-dioxabicyclo[2.2.1]heptan-3-yl]purin-6-yl]benzamide
XHEVZGBLRSIPCO-DZGFXGBPSA-N
C[C@H]1[C@]2([C@H]([C@@H](O1)[C@@H](O2)N3C=NC4=C(N=CN=C43)NC(=O)C5=CC=CC=C5)OP(N(C(C)C)C(C)C)OCCC#N)COC(C6=CC=CC=C6)(C7=CC=C(C=C7)OC)C8=CC=C(C=C8)OC