Amino-modified Nucleosides
2-Amino-3',5'-di-O-acetyl-N6,N6-dimethyl-2'-O-methyladenosine
Quick view. 2-Amino-3',5'-di-O-acetyl-N6,N6-dimethyl-2'-O-methyladenosine is listed for research-use inquiry under Amino-modified Nucleosides. Its identity is controlled by the retained exact structure and product-form evidence because no public CAS Registry Number is assigned. A public CAS number is not assigned for this exact form. Catalog target purity: ≥98%. Availability: Inquiry only — contact BX Lab to confirm current availability.
Product profile
2-Amino-3',5'-di-O-acetyl-N6,N6-dimethyl-2'-O-methyladenosine is classified as amino-modified nucleosides (Formula C17H24N6O6; molecular weight 408.41).
2-Amino-3',5'-di-O-acetyl-N6,N6-dimethyl-2'-O-methyladenosine provides a reactive functional group for conjugation, immobilization or linker-extension studies.
For 2-Amino-3',5'-di-O-acetyl-N6,N6-dimethyl-2'-O-methyladenosine, functional handles may require orthogonal protection, pH control and rapid purification to avoid hydrolysis, oxidation or cross-reaction.
Physicochemical data
| CAS status | No public CAS assigned |
|---|---|
| Identity control | Reviewed exact name, structure, and product form |
| InChIKey | PNOUIJPTMAKPKH-XNIJJKJLSA-N |
| InChI | InChI=1S/C17H24N6O6/c1-8(24)27-6-10-12(28-9(2)25)13(26-5)16(29-10)23-7-19-11-14(22(3)4)20-17(18)21-15(11)23/h7,10,12-13,16H,6H2,1-5H3,(H2,18,20,21)/t10-,12-,13-,16-/m1/s1 |
| SMILES | CC(=O)OC[C@@H]1[C@H]([C@H]([C@@H](O1)N2C=NC3=C2N=C(N=C3N(C)C)N)OC)OC(=O)C |
| Canonical SMILES | CC(=O)OC[C@@H]1[C@H]([C@H]([C@@H](O1)N2C=NC3=C2N=C(N=C3N(C)C)N)OC)OC(=O)C |
| PubChem CID | 170902280 |
Release documentation
The current specification defines the analytical method and acceptance criteria; the released lot result is reported on the CoA.
Additional HPLC, MS or NMR documentation can be agreed during technical review where available.
Product-specific evaluation notes
Potential advantages
- Reactive handles make the product adaptable across dye-labeling, surface-coupling and ligand-conjugation workflows.
- 2′-O-methyl groups are widely used to increase nuclease resistance and modulate hybridization behavior.
Method limitations
- Functional handles may require orthogonal protection, pH control and rapid purification to avoid hydrolysis, oxidation or cross-reaction.
- Excessive or poorly positioned substitution can reduce desired enzyme interactions or activity in some assay formats.
These points describe 2-Amino-3',5'-di-O-acetyl-N6,N6-dimethyl-2'-O-methyladenosine or its named chemical feature. Broader product-family guidance is maintained on the category page.
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Frequently asked questions
Can the package size for 2-Amino-3',5'-di-O-acetyl-N6,N6-dimethyl-2'-O-methyladenosine be customized?
Yes. Share the initial quantity, expected future scale, delivery timeline and packaging preference for review.
What information should be included in a quote request?
Quote catalog number BX-AMN-0159, the intended research workflow, required quantity and any additional HPLC, MS or NMR documentation needed.
Product-family literature
These publications provide peer-reviewed context for the Amino-modified Nucleosides product family and its named chemistry. They are background reading only, not evidence for the exact product, supplied form, lot specification, availability or performance.
Technology platforms
Catalog-derived platform membership for navigating related chemistry and verifiable product sets.