This compound is a research reagent employed in oligonucleotide synthesis. It features a protected purine nucleoside structure with a phosphoramidite group, making it suitable for use in automated DNA/RNA synthesis processes.
Content scope: Information here supports chemical identification and industrial supply, research, and manufacturing contexts. It is not a therapeutic claim, medical advice, or drug-use instructions.
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N-[9-[(2R,3R,4R,5R)-5-[(1R)-1-[bis(4-methoxyphenyl)-phenyl-methoxy]ethyl]-4-[2-cyanoethoxy-(diisopropylamino)phosphanyl]oxy-3-fluoro-tetrahydrofuran-2-yl]purin-6-yl]benzamide
research compound
2'-OMe PAC Abeta-cyanoethyl phosphoramidite
research compound
5'-O-[Bis(4-methoxyphenyl)(phenyl)methyl]-2'-O-methyluridine
research compound
2'-O-Methyl-5'-O-DMT-pseudoUridine 3'-CE phosphoramidite
research compound
MORPHOLINO G SUBUNIT
research compound
(Z)-N'-{9-[(2R,4S,5R)-5-{[bis(4-methoxyphenyl)(phenyl)methoxy]methyl}-4-({[bis(propan-2-yl)amino](2-cyanoethoxy)phosphanyl}oxy)oxolan-2-yl]-9H-purin-6-yl}-N,N-dimethylmethanimidamide
research compound
5-Cyanothiophene-2-boronic acid
research compound
Tert-butyl N-(benzotriazol-1-ylmethyl)carbamate
research compound
N-[9-[(2R,3R,4R,5R)-5-[(1R)-1-[bis(4-methoxyphenyl)-phenylmethoxy]ethyl]-4-[2-cyanoethoxy-[di(propan-2-yl)amino]phosphanyl]oxy-3-methoxyoxolan-2-yl]purin-6-yl]benzamide
BCWJFMZZTZLRMI-MUGUQXIBSA-N
C[C@H]([C@@H]1[C@H]([C@H]([C@@H](O1)N2C=NC3=C(N=CN=C32)NC(=O)C4=CC=CC=C4)OC)OP(N(C(C)C)C(C)C)OCCC#N)OC(C5=CC=CC=C5)(C6=CC=C(C=C6)OC)C7=CC=C(C=C7)OC
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