2'-F-ANA Phosphoramidites
N4-Benzoyl-5'-O-DMTr-2'-deoxy-2'-fluoro-beta-D-arabinocytidine-3'-CE phosphoramidite
Quick view. A protected 2'-F-ANA cytidine building block bearing N4-benzoyl and 5'-O-DMTr groups with a 3'-cyanoethyl N,N-diisopropylphosphoramidite functionality. CAS 1404463-12-2. 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
N4-Benzoyl-5'-O-DMTr-2'-deoxy-2'-fluoro-beta-D-arabinocytidine-3'-CE phosphoramidite is classified as 2'-f-ana phosphoramidites (Formula C46H51FN5O8P; molecular weight 851.90).
N4-Benzoyl-5'-O-DMTr-2'-deoxy-2'-fluoro-beta-D-arabinocytidine-3'-CE phosphoramidite — Identity-defined 2'-F-ANA-dC(Bz) phosphoramidite for research workflows involving solid-phase oligonucleotide synthesis.
For N4-Benzoyl-5'-O-DMTr-2'-deoxy-2'-fluoro-beta-D-arabinocytidine-3'-CE phosphoramidite, coupling, deprotection and biological performance remain sequence- and position-dependent.
Names and search terms
Confirmed or normalized name variants
- 2'-F-ANA-dC(Bz) phosphoramidite
- 2'-Fluoro-2'-deoxy-ara-C(Bz)-3'-phosphoramidite
- ANA 2'-F C(Bz) amidite
Useful catalog search terms
- CAS 1404463-12-2
Physicochemical data
| Nucleoside | 2'-Deoxy-2'-fluoro-beta-D-arabinocytidine |
|---|---|
| Base protection | N4-Benzoyl |
| 5'-Protecting group | DMTr |
| 3'-Coupling group | 2-Cyanoethyl N,N-diisopropylphosphoramidite |
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
- 2′-fluoro motifs can improve nuclease resistance while preserving RNA-like geometry in many sequence contexts.
Method limitations
- Coupling, deprotection and biological performance remain sequence- and position-dependent.
These points describe N4-Benzoyl-5'-O-DMTr-2'-deoxy-2'-fluoro-beta-D-arabinocytidine-3'-CE phosphoramidite 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 N4-Benzoyl-5'-O-DMTr-2'-deoxy-2'-fluoro-beta-D-arabinocytidine-3'-CE phosphoramidite 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-2FAP-0005 and CAS 1404463-12-2, the intended research workflow, required quantity and any additional HPLC, MS or NMR documentation needed.
Feature and workflow background
These publications discuss a broader chemistry feature or workflow identified from the catalog name or product family. They are background reading only, not evidence for the exact BX Lab product, supplied form, lot specification, availability or performance.
Technology platforms
Catalog-derived platform membership for navigating related chemistry and verifiable product sets.