This compound is a modified nucleoside derivative featuring a protected adenine base and a phosphoramidite group, commonly used in oligonucleotide synthesis. Its complex structure includes multiple aromatic rings, ether linkages, and a chiral fluorinated sugar moiety, reflecting its role as a building block for nucleic acid chemistry.
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CAS 2227293-35-6
N-[9-[(2R,3R,4R,5R)-5-[[bis(4-methoxyphenyl)-phenylmethoxy]methyl]-4-[2-cyanoethoxy-[di(propan-2-yl)amino]phosphanyl]oxy-3-fluorooxolan-2-yl]purin-6-yl]benzamide
Pharmaceutical intermediate for oligonucleotide synthesis
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 reagent
6-bromo-2-methyl-3-nitropyridine
n.a
1,1-difluoro-2-methyl-3-(2-methyloxolan-3-yl)propan-2-amine
n.a
2-Chloro-4-(4-(naphthalen-1-yl)phenyl)-6-phenyl-1,3,5-triazine
n.a
2-(3-Bromo-4-fluorophenyl)-4,6-diphenyl-1,3,5-triazine
n.a
N-[9-[4-[bis(4-methoxyphenyl)-phenylmethoxy]-5-[[2-cyanoethoxy-[di(propan-2-yl)amino]phosphanyl]oxymethyl]-3-fluorooxolan-2-yl]purin-6-yl]benzamide
NZDMBUCNULHYQM-UHFFFAOYSA-N
CC(C)N(C(C)C)P(OCCC#N)OCC1C(C(C(O1)N2C=NC3=C(N=CN=C32)NC(=O)C4=CC=CC=C4)F)OC(C5=CC=CC=C5)(C6=CC=C(C=C6)OC)C7=CC=C(C=C7)OC
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