Halogenated Nucleosides
N6-(3-Trifluoromethylbenzyl)adenosine
Quick view. Adenosine derivative bearing a 3-trifluoromethylbenzyl substituent at N6. CAS 23661-03-2. Catalog target purity: By inquiry. Availability: Inquiry only — contact OROGO to confirm current availability.
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Product profile
N6-(3-Trifluoromethylbenzyl)adenosine is classified as halogenated nucleosides (Formula C18H18F3N5O4; molecular weight 425.36 g/mol).
N6-(3-Trifluoromethylbenzyl)adenosine — Reported as ligand L4 in the synthesis of N6-substituted adenosine iron complexes.
For N6-(3-Trifluoromethylbenzyl)adenosine, coupling, deprotection and biological performance remain sequence- and position-dependent.
Names and search terms
Useful catalog search terms
- 23661-03-2
Physicochemical data
| Nucleoside | Adenosine |
|---|---|
| Substitution pattern | N6-(3-trifluoromethylbenzyl) |
| Stereochemical scope | Beta-D-ribofuranosyl configuration |
| InChIKey | SDQKDCSBWUSBDO-LSCFUAHRSA-N |
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 N6-(3-Trifluoromethylbenzyl)adenosine or its named chemical feature. Broader product-family guidance is maintained on the category page.
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Product-relevant literature
The publications below discuss named chemistry or a structural feature represented by this product. They provide scientific context only and are not an OROGO lot specification or product-performance claim.
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