Amino-modified Nucleosides
2-Amino-9-(3-deoxy-3-fluoro-beta-D-ribofuranosyl)-9H-purine
Quick view. An amino-modified, 3'-deoxy-3'-fluoro purine nucleoside building block for structure-specific nucleoside synthesis research. CAS 1612192-04-7. Catalog target purity: ≥98%. Availability: Inquiry only; contact BX Lab to confirm current availability.
Structure and identity
The structure drawing for this item is being finalized. Use the CAS number and machine-readable identifiers below to confirm the requested protecting groups, stereochemistry, salt or counterion and hydration state before ordering.
CAS, molecular formula, SMILES or InChI data are shown below when available.
We withhold a drawing when a related compound, alternate salt or incompletely specified stereoisomer could be mistaken for the requested material.
Agreed identity and purity criteria are documented in the quotation, specification and lot-specific data package.
Product profile
2-Amino-9-(3-deoxy-3-fluoro-beta-D-ribofuranosyl)-9H-purine is classified as amino-modified nucleosides (Formula C10H12FN5O3; molecular weight 269.232).
2-Amino-9-(3-deoxy-3-fluoro-beta-D-ribofuranosyl)-9H-purine — Amino-modified, fluorinated purine nucleoside building block for structure-specific nucleoside synthesis research.
For 2-Amino-9-(3-deoxy-3-fluoro-beta-D-ribofuranosyl)-9H-purine, functional handles may require orthogonal protection, pH control and rapid purification to avoid hydrolysis, oxidation or cross-reaction.
Names and search terms
Confirmed or normalized name variants
- 9H-Purin-2-amine, 9-(3-deoxy-3-fluoro-beta-D-ribofuranosyl)-
- (2R,3S,4S,5R)-2-(2-Amino-9H-purin-9-yl)-4-fluoro-5-(hydroxymethyl)tetrahydrofuran-3-ol
Useful catalog search terms
- CAS 1612192-04-7
Physicochemical data
| Sugar modification | 3'-deoxy-3'-fluoro |
|---|---|
| Purine substitution | 2-amino |
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′-fluoro motifs can improve nuclease resistance while preserving RNA-like geometry in many sequence contexts.
Method limitations
- Functional handles may require orthogonal protection, pH control and rapid purification to avoid hydrolysis, oxidation or cross-reaction.
- Coupling, deprotection and biological performance remain sequence- and position-dependent.
These points describe 2-Amino-9-(3-deoxy-3-fluoro-beta-D-ribofuranosyl)-9H-purine 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-9-(3-deoxy-3-fluoro-beta-D-ribofuranosyl)-9H-purine 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-0032 and CAS 1612192-04-7, 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.