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5/'-O-(4,4-Dimethoxytrityl)-2/'-O-methyl-N-isobutyrylguanosine-3/'-(2-cyanoethyl-N,N-diisopropyl)pho
For research use only. Not for therapeutic Use.
5′-O-(4,4-Dimethoxytrityl)-2′-O-methyl-N-isobutyrylguanosine-3′-(2-cyanoethyl-N,N-diisopropyl)phosphoramidite(Cat No.:M101952)is a modified guanosine derivative used in oligonucleotide synthesis. The dimethoxytrityl (DMT) group protects the 5’-hydroxyl, while the 2’-O-methyl modification enhances stability against nucleases. The isobutyryl group protects the guanine base during synthesis. This compound is key in constructing RNA and DNA oligonucleotides for research, diagnostics, and therapeutic applications. The cyanoethyl phosphoramidite functionality enables efficient coupling during automated oligonucleotide synthesis, making it crucial for the production of high-fidelity nucleic acids with enhanced stability and modified properties.
Catalog Number | M101952 |
CAS Number | 150780-67-9 |
Molecular Formula | C45H56N7O9P |
Purity | ≥95% |
Target | DNA/RNA Synthesis |
Storage | 2-8°C |
IUPAC Name | N-[9-[(2R,3R,4R,5R)-5-[[bis(4-methoxyphenyl)-phenylmethoxy]methyl]-4-[2-cyanoethoxy-[di(propan-2-yl)amino]phosphanyl]oxy-3-methoxyoxolan-2-yl]-6-oxo-1H-purin-2-yl]-2-methylpropanamide |
InChI | InChI=1S/C45H56N7O9P/c1-28(2)41(53)49-44-48-40-37(42(54)50-44)47-27-51(40)43-39(57-9)38(61-62(59-25-13-24-46)52(29(3)4)30(5)6)36(60-43)26-58-45(31-14-11-10-12-15-31,32-16-20-34(55-7)21-17-32)33-18-22-35(56-8)23-19-33/h10-12,14-23,27-30,36,38-39,43H,13,25-26H2,1-9H3,(H2,48,49,50,53,54)/t36-,38-,39-,43-,62?/m1/s1 |
InChIKey | IRRDHRZUOZNWDJ-MLLDKZSOSA-N |
SMILES | CC(C)C(=O)NC1=NC2=C(C(=O)N1)N=CN2C3C(C(C(O3)COC(C4=CC=CC=C4)(C5=CC=C(C=C5)OC)C6=CC=C(C=C6)OC)OP(N(C(C)C)C(C)C)OCCC#N)OC |