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for DNA synthesis, Suitable for molecular biology, ≥98%(mixture of isomers) for DNA synthesis,Suitable for molecular biology for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Protected from light,Store at -20°C,Argon charged Ships Ice chest + Ice pads Check lot-specific COA for exact specifications.
SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
LNA-A(Bz) amidite can be used for synthesis of ASOs (antisense oligonucleotides).
| Canonical Smiles | CC(C)N(C(C)C)P(OCCC#N)OC1C2C(OC1(CO2)COC(C3=CC=CC=C3)(C4=CC=C(C=C4)OC)C5=CC=C(C=C5)OC)N6C=NC7=C(N=CN=C76)NC(=O)C8=CC=CC=C8 |
|---|---|
| IUPAC Name | N-[9-[(1R,3R,4R,7S)-1-[[bis(4-methoxyphenyl)-phenylmethoxy]methyl]-7-[2-cyanoethoxy-[di(propan-2-yl)amino]phosphanyl]oxy-2,5-dioxabicyclo[2.2.1]heptan-3-yl]purin-6-yl]benzamide |
| InChIKey | HPIDKMAOZZZGOP-LIUGLABVSA-N |
| INCHI | 1S/C48H52N7O8P/c1-32(2)55(33(3)4)64(61-27-13-26-49)63-42-41-46(54-31-52-40-43(50-30-51-44(40)54)53-45(56)34-14-9-7-10-15-34)62-47(42,28-59-41)29-60-48(35-16-11-8-12-17-35,36-18-22-38(57-5)23-19-36)37-20-24-39(58-6)25-21-37/h7-12,14-25,30-33,41-42,46H,13,27-29H2,1-6H3,(H,50,51,53,56)/t41-,42+,46-,47-,64?/m1/s1 |
| Isomeric SMILES | CC(C)N(C(C)C)P(OCCC#N)O[C@H]1[C@@H]2[C@@H](O[C@]1(CO2)COC(C3=CC=CC=C3)(C4=CC=C(C=C4)OC)C5=CC=C(C=C5)OC)N6C=NC7=C(N=CN=C76)NC(=O)C8=CC=CC=C8 |
| Alternate CAS | 206055-79-0 |
| Molecular Weight | 885.96 |
Comprehensive hazard, handling, storage, and regulatory compliance document.
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View spec sheet →Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Benzenoids |
| Class | Triphenyl compounds |
| Subclass | Not available |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Triphenyl compounds |
| Alternative Parents | Nucleoside and nucleotide analogues Glycosylamines Benzamides Benzylethers Purines and purine derivatives Anisoles Benzoyl derivatives Phenoxy compounds Methoxybenzenes Alkyl aryl ethers N-substituted imidazoles Monosaccharides Imidolactams 1,4-dioxanes Pyrimidines and pyrimidine derivatives Heteroaromatic compounds Oxolanes Secondary carboxylic acid amides Nitriles Azacyclic compounds Dialkyl ethers Oxacyclic compounds Hydrocarbon derivatives Organic oxides Organopnictogen compounds |
| Molecular Framework | Aromatic heteropolycyclic compounds |
| Substituents | Triphenyl compound - N-glycosyl compound - Glycosyl compound - Imidazopyrimidine - Purine - Benzylether - Benzamide - Benzoic acid or derivatives - Phenoxy compound - Phenol ether - Anisole - Methoxybenzene - Benzoyl - Alkyl aryl ether - Imidolactam - Para-dioxane - Pyrimidine - Monosaccharide - N-substituted imidazole - Monocyclic benzene moiety - Oxolane - Azole - Imidazole - Heteroaromatic compound - Carboxamide group - Secondary carboxylic acid amide - Carbonitrile - Nitrile - Oxacycle - Azacycle - Organoheterocyclic compound - Carboxylic acid derivative - Dialkyl ether - Ether - Cyanide - Organic nitrogen compound - Organic oxide - Hydrocarbon derivative - Organopnictogen compound - Organic oxygen compound - Organooxygen compound - Organonitrogen compound - Aromatic heteropolycyclic compound |
| Description | This compound belongs to the class of organic compounds known as triphenyl compounds. These are aromatic compounds containing a triphenyl moiety. |
| External Descriptors | Not available |
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Date | Item |
|---|---|---|---|
| Certificate of Analysis | Apr 29, 2025 | D778067 | |
| Certificate of Analysis | Apr 29, 2025 | D778067 | |
| Certificate of Analysis | Apr 29, 2025 | D778067 | |
| Certificate of Analysis | Apr 29, 2025 | D778067 |
| Sensitivity | Moisture sensitive; Light sensitive |
|---|
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