Amino-modified Nucleosides
Uridine-5-(N-Fmoc-methylamino)-acetyl (9-fluorenylmethyl) ester
Quick view. Uridine-5-(N-Fmoc-methylamino)-acetyl (9-fluorenylmethyl) ester is listed for research-use inquiry under Amino-modified Nucleosides. Its identity is controlled by the retained exact structure and product-form evidence because no public CAS Registry Number is assigned. A public CAS number is not assigned for this exact form. Catalog target purity: ≥98%. Availability: Inquiry only — contact BX Lab to confirm current availability.
Product profile
Uridine-5-(N-Fmoc-methylamino)-acetyl (9-fluorenylmethyl) ester is classified as amino-modified nucleosides (Formula C41H37N3O10; molecular weight 731.70 g/mol).
Uridine-5-(N-Fmoc-methylamino)-acetyl (9-fluorenylmethyl) ester provides a reactive functional group for conjugation, immobilization or linker-extension studies.
For Uridine-5-(N-Fmoc-methylamino)-acetyl (9-fluorenylmethyl) ester, functional handles may require orthogonal protection, pH control and rapid purification to avoid hydrolysis, oxidation or cross-reaction.
Physicochemical data
| CAS status | No public CAS assigned |
|---|---|
| Identity control | Reviewed exact name, structure, and product form |
| InChIKey | VRXIUJHNXIFTQB-CBOKRJPRSA-N |
| InChI | InChI=1S/C41H37N3O10/c45-20-34-36(47)37(48)39(54-34)44-18-23(38(49)42-40(44)50)17-43(41(51)53-22-33-30-15-7-3-11-26(30)27-12-4-8-16-31(27)33)19-35(46)52-21-32-28-13-5-1-9-24(28)25-10-2-6-14-29(25)32/h1-16,18,32-34,36-37,39,45,47-48H,17,19-22H2,(H,42,49,50)/t34-,36-,37-,39-/m1/s1 |
| SMILES | C1=CC=C2C(=C1)C(C3=CC=CC=C32)COC(=O)CN(CC4=CN(C(=O)NC4=O)[C@H]5[C@@H]([C@@H]([C@H](O5)CO)O)O)C(=O)OCC6C7=CC=CC=C7C8=CC=CC=C68 |
| Canonical SMILES | C1=CC=C2C(=C1)C(C3=CC=CC=C32)COC(=O)CN(CC4=CN(C(=O)NC4=O)[C@H]5[C@@H]([C@@H]([C@H](O5)CO)O)O)C(=O)OCC6C7=CC=CC=C7C8=CC=CC=C68 |
| PubChem CID | 170902491 |
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.
Method limitations
- Functional handles may require orthogonal protection, pH control and rapid purification to avoid hydrolysis, oxidation or cross-reaction.
These points describe Uridine-5-(N-Fmoc-methylamino)-acetyl (9-fluorenylmethyl) ester 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 Uridine-5-(N-Fmoc-methylamino)-acetyl (9-fluorenylmethyl) ester 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-0247, 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.