Amino-modified Nucleosides
5'-Azido-3'-O-(t-butyldimethylsilyl)-1-(2'-O,4'-C-methylene-beta-D-ribofuranosyl)-uridineacil
Quick view. We supply 5'-Azido-3'-O-(t-butyldimethylsilyl)-1-(2'-O,4'-C-methylene-beta-D-ribofuranosyl)-uridineacil as a specialty product for nucleic acid chemistry and oligonucleotide research workflows. A public CAS number is not assigned for this exact form. 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'-Azido-3'-O-(t-butyldimethylsilyl)-1-(2'-O,4'-C-methylene-beta-D-ribofuranosyl)-uridineacil is classified as nucleoside or protected nucleoside intermediate.
5'-Azido-3'-O-(t-butyldimethylsilyl)-1-(2'-O,4'-C-methylene-beta-D-ribofuranosyl)-uridineacil can serve as a starting material, protected intermediate or analytical comparator in nucleoside and nucleotide route development.
For 5'-Azido-3'-O-(t-butyldimethylsilyl)-1-(2'-O,4'-C-methylene-beta-D-ribofuranosyl)-uridineacil, copper-catalyzed, copper-free or inverse-electron-demand click conditions can affect sensitive oligonucleotides differently; residual metal, solvent and purification strategy should be controlled.
Names and search terms
Useful catalog search terms
- Nucleoside or protected nucleoside intermediate
- azide click handle
- amine functionality
- Amino-modified Nucleosides
Physicochemical data
| Key chemistry motifs | azide click handle; amine functionality |
|---|
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
- 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
- Click-compatible handles separate oligonucleotide synthesis from late-stage labeling, which helps screen multiple payloads from a common intermediate.
- Reactive handles make the product adaptable across dye-labeling, surface-coupling and ligand-conjugation workflows.
Method limitations
- Copper-catalyzed, copper-free or inverse-electron-demand click conditions can affect sensitive oligonucleotides differently; residual metal, solvent and purification strategy should be controlled.
- Functional handles may require orthogonal protection, pH control and rapid purification to avoid hydrolysis, oxidation or cross-reaction.
These points describe 5'-Azido-3'-O-(t-butyldimethylsilyl)-1-(2'-O,4'-C-methylene-beta-D-ribofuranosyl)-uridineacil 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'-Azido-3'-O-(t-butyldimethylsilyl)-1-(2'-O,4'-C-methylene-beta-D-ribofuranosyl)-uridineacil 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-0217, the intended research workflow, required quantity and any additional HPLC, MS or NMR documentation needed.
Product-relevant literature
The publications below discuss 5'-Azido-3'-O-(t-butyldimethylsilyl)-1-(2'-O,4'-C-methylene-beta-D-ribofuranosyl)-uridineacil or the named structural feature represented by this product.