Amino-modified Nucleosides
5-(N-t-Butyloxycarbonylmethyl)-N-(trifluoroacetyl) aminomethyl)-2-thiouridine
Quick view. We supply 5-(N-t-Butyloxycarbonylmethyl)-N-(trifluoroacetyl) aminomethyl)-2-thiouridine as a specialty product for nucleic acid chemistry and oligonucleotide research workflows. CAS 89129-10-2. Catalog target purity: Specification on request.
Structure confirmation
This item requires structure confirmation before quotation. Send the target structure, CAS number, SMILES, InChI or drawing for our technical review.
Canonical name plus a structure drawing, SMILES, InChI or unambiguous CAS number.
Protecting groups, stereochemistry, salt or counterion, hydration and requested form.
Agreed identity and purity criteria are documented in the quotation, specification and lot-specific data package.
Product profile
5-(N-t-Butyloxycarbonylmethyl)-N-(trifluoroacetyl) aminomethyl)-2-thiouridine is classified as nucleoside or protected nucleoside intermediate.
5-(N-t-Butyloxycarbonylmethyl)-N-(trifluoroacetyl) aminomethyl)-2-thiouridine can serve as a starting material, protected intermediate or analytical comparator in nucleoside and nucleotide route development.
For 5-(N-t-Butyloxycarbonylmethyl)-N-(trifluoroacetyl) aminomethyl)-2-thiouridine, functional handles may require orthogonal protection, pH control and rapid purification to avoid hydrolysis, oxidation or cross-reaction.
Names and search terms
Useful catalog search terms
- CAS 89129-10-2
- Nucleoside or protected nucleoside intermediate
- amine functionality
- Amino-modified Nucleosides
Physicochemical data
| Key chemistry motifs | amine functionality |
|---|---|
| Density | 1.47±0.1 g/cm3(Predicted) |
| pKa | 6.70±0.23(Predicted) |
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.
Additional application examples
- β-D-Ribofuranose analogue 1 is a nucleoside compound. β-D-Ribofuranose analogue 1 can be used for RNA synthesis.
- Typical work includes protection/deprotection studies, phosphorylation or phosphitylation route scouting and impurity identification.
- The material can support medicinal-chemistry analog preparation and process-development feasibility studies.
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-t-Butyloxycarbonylmethyl)-N-(trifluoroacetyl) aminomethyl)-2-thiouridine 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-t-Butyloxycarbonylmethyl)-N-(trifluoroacetyl) aminomethyl)-2-thiouridine 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-0241 and CAS 89129-10-2, the intended research workflow, required quantity and any additional HPLC, MS or NMR documentation needed.
Product-family literature
The publications below provide peer-reviewed context for the Amino-modified Nucleosides product family and its named chemistry.