Amino-modified Nucleosides
5-[(N-Isopentenyl-N-trifluoroacetyl)aminomethyl]uridine
Quick view. A protected amino-side-chain uridine building block for structure-specific modified-nucleoside research. CAS 1613530-43-0. Catalog target purity: ≥98%. Availability: Inquiry only — contact BX Lab to confirm current availability.
![Chemical structure of 5-[(N-Isopentenyl-N-trifluoroacetyl)aminomethyl]uridine](/structures/7eb20c380fce69fe.svg)
Product profile
5-[(N-Isopentenyl-N-trifluoroacetyl)aminomethyl]uridine is classified as amino-modified nucleosides (Formula C17H22F3N3O7; molecular weight 437.37).
5-[(N-Isopentenyl-N-trifluoroacetyl)aminomethyl]uridine — Protected amino-side-chain uridine building block for structure-specific modified-nucleoside research.
For 5-[(N-Isopentenyl-N-trifluoroacetyl)aminomethyl]uridine, 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
- Uridine, 5-[[(3-methyl-2-buten-1-yl)(2,2,2-trifluoroacetyl)amino]methyl]-
Useful catalog search terms
- CAS 1613530-43-0
- isopentenyl trifluoroacetyl aminomethyl uridine
- NVDLHYHKFKHIDC-HKUMRIAESA-N
- PubChem CID 154704825
Physicochemical data
| Nucleoside modification | 5-aminomethyl side chain |
|---|---|
| Side-chain substituents | N-isopentenyl; N-trifluoroacetyl |
| PubChem CID | 154704825 |
| InChIKey | NVDLHYHKFKHIDC-HKUMRIAESA-N |
| InChI | InChI=1S/C17H22F3N3O7/c1-8(2)3-4-22(15(28)17(18,19)20)5-9-6-23(16(29)21-13(9)27)14-12(26)11(25)10(7-24)30-14/h6,10-12,14,24-26H,1,3-5,7H2,2H3,(H,21,27,29)/t10-,11-,12-,14-/m1/s1 |
| SMILES | CC(=C)CCN(CC1=CN(C(=O)NC1=O)[C@H]2[C@@H]([C@@H]([C@H](O2)CO)O)O)C(=O)C(F)(F)F |
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 5-[(N-Isopentenyl-N-trifluoroacetyl)aminomethyl]uridine 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 5-[(N-Isopentenyl-N-trifluoroacetyl)aminomethyl]uridine 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-0147 and CAS 1613530-43-0, 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.