Intermediates
5-Fluorouracil-1-yl acetic acid
Quick view. We supply 5-Fluorouracil-1-yl acetic acid as a specialty product for nucleic acid chemistry and oligonucleotide research workflows. CAS 56059-30-4. Catalog target purity: Specification on request.
Structure and identity
The structure drawing for this item is being finalized. Use the CAS number and machine-readable identifiers below to confirm the requested protecting groups, stereochemistry, salt or counterion and hydration state before ordering.
CAS, molecular formula, SMILES or InChI data are shown below when available.
We withhold a drawing when a related compound, alternate salt or incompletely specified stereoisomer could be mistaken for the requested material.
Agreed identity and purity criteria are documented in the quotation, specification and lot-specific data package.
Product profile
5-Fluorouracil-1-yl acetic acid is classified as specialty research-use chemical building block (Formula C6H5FN2O4; molecular weight 188.11).
5-Fluorouracil-1-yl acetic acid can be used as a defined research input for chemistry feasibility, analytical method development and material comparison.
For 5-Fluorouracil-1-yl acetic acid, storage: Sealed in dry,Room Temperature.
Names and search terms
Confirmed or normalized name variants
- 5-Fluoro-3,4-dihydro-2,4-dioxo-1(2H)-PyriMidineacetic Acid
- 1(2H)-Pyrimidineacetic acid, 5-fluoro-3,4-dihydro-2,4-dioxo-
- 2-(5-Fluoro-2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)acetic acid
Useful catalog search terms
- CAS 56059-30-4
- Specialty research-use chemical building block
- Intermediates
Physicochemical data
| Melting point | 253-256 °C |
|---|---|
| Density | 1.69±0.1 g/cm3(Predicted) |
| pKa | 3.81±0.10(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
- Typical qualification includes identity, purity method, storage, handling and downstream workflow compatibility.
- Related analogs, impurity standards and custom quantities can be reviewed for project-specific research needs.
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 5-Fluorouracil-1-yl acetic acid or its named chemical feature. Broader product-family guidance is maintained on the category page.
Related products
(2'OMe-5'PP-A)pG TEA Salt
Intermediates · CAS: N/A
BX-INTE-0002(2'OMe-5'p(S)-A)pG TEA Salt
Intermediates · CAS: 2295879-58-0
BX-INTE-0003(2'OMe-5'p-A)p(S)G TEA Salt
Intermediates · CAS: N/A
BX-INTE-0004(2'OMe-5'p-A)pG TEA Salt
Intermediates · CAS: 62828-60-8
BX-INTE-0005(2'OMe-5'p-A)pU TEA Salt
Intermediates · CAS: 2956650-76-1
BX-INTE-0006(2'OMe-5'p-G)pG TEA Salt
Intermediates · CAS: 2638447-65-9
Frequently asked questions
Can the package size for 5-Fluorouracil-1-yl acetic acid 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-INTE-0086 and CAS 56059-30-4, the intended research workflow, required quantity and any additional HPLC, MS or NMR documentation needed.
Product-relevant literature
The publications below discuss 5-Fluorouracil-1-yl acetic acid or the named structural feature represented by this product.