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(2S,3S,5R)-N-(2-((1S,2S,3S,5R,6R)-3,5-DIAZIDO-2-((2S,3R,4R,5S,6R)-3-AZIDO-6-(AZIDOMETHYL)-4,5-DIHYDROXYTETRAHYDRO-2H-PYRAN-2-YLOXY)-6-HYDROXYCYCLOHEXYLAMINO)ETHYL)-3-HYDROXY-5-(5-METHYL-2,4-DIOXO-3,4-DIHYDROPYRIMIDIN-1(2H)-YL)TETRAHYDROFURAN-2-CARBOXAMIDE CAS NO 948916-26-5
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CAS No.:948916-26-5
Grade:Pharmacy Grade
Content:99.9%
Brand:Customizable
Packaging:Customizable
Description
(2S,3S,5R)-N-(2-((1S,2S,3S,5R,6R)-3,5-DIAZIDO-2-((2S,3R,4R,5S,6R)-3-AZIDO-6-(AZIDOMETHYL)-4,5-DIHYDROXYTETRAHYDRO-2H-PYRAN-2-YLOXY)-6-HYDROXYCYCLOHEXYLAMINO)ETHYL)-3-HYDROXY-5-(5-METHYL-2,4-DIOXO-3,4-DIHYDROPYRIMIDIN-1(2H)-YL)TETRAHYDROFURAN-2-CARBOXAMIDE is a sophisticated, multi-functional nucleoside analog derivative designed for advanced pharmaceutical research and development. This compound is of significant interest due to its complex, stereochemically defined structure, which incorporates multiple azido groups and a thymine base, making it a valuable click chemistry precursor and a key intermediate in the synthesis of novel antiviral and anticancer agents. It is primarily utilized by pharmaceutical R&D laboratories and biotech companies focused on developing next-generation therapeutics, particularly in the fields of nucleoside-based prodrugs and targeted drug delivery systems.
Application
- Pharmaceutical Intermediate: Serves as a critical building block in the synthesis of novel nucleoside analog prodrugs with potential antiviral or anticancer activity.
- Click Chemistry Reagent: The multiple azido (-N3) functional groups enable efficient, site-specific bioconjugation via copper-catalyzed azide-alkyne cycloaddition (CuAAC) for labeling and drug targeting.
- Antiviral Research: Used as a precursor in the development of experimental therapeutics targeting viral polymerases (e.g., for HIV, Hepatitis).
- Oncology Drug Discovery: Investigated as an intermediate for creating compounds that interfere with DNA/RNA synthesis in rapidly dividing cancer cells.
- Bioconjugation & Probe Development: Facilitates the creation of fluorescent or affinity probes for studying biological pathways and target engagement.
- Academic & Institutional Research: Employed in universities and research institutes for studying nucleoside chemistry, enzyme inhibition, and structure-activity relationships (SAR).
Basic Information
| Product Name | (2S,3S,5R)-N-(2-((1S,2S,3S,5R,6R)-3,5-DIAZIDO-2-((2S,3R,4R,5S,6R)-3-AZIDO-6-(AZIDOMETHYL)-4,5-DIHYDROXYTETRAHYDRO-2H-PYRAN-2-YLOXY)-6-HYDROXYCYCLOHEXYLAMINO)ETHYL)-3-HYDROXY-5-(5-METHYL-2,4-DIOXO-3,4-DIHYDROPYRIMIDIN-1(2H)-YL)TETRAHYDROFURAN-2-CARBOXAMIDE |
| CAS No. | 948916-26-5 |
| Molecular Formula | C24H34N14O11 |
| Molecular Weight | 694.62 g/mol |
| Synonyms | 1-(3-Azido-4,5-dihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)-5-methylpyrimidine-2,4(1H,3H)-dione derivative; Multi-azido functionalized thymidine analog; Azido-modified nucleoside intermediate; CAS 948916-26-5; Click chemistry nucleoside precursor; Thymidine triazido derivative; Advanced pharmaceutical intermediate 948916-26-5 |
| EINECS | Contact for details |
Quality Control
This high-value intermediate is manufactured under strict quality control protocols to ensure batch-to-batch consistency and purity suitable for research applications. Our quality assurance includes comprehensive analytical characterization using techniques such as HPLC, NMR, and MS to confirm identity and purity. A detailed Certificate of Analysis (COA) is provided with each batch, documenting critical parameters. While not typically governed by compendial standards like USP/EP at this research stage, our production adheres to cGMP principles where applicable to support its use in pre-clinical development.
Storage
Preserve in a tightly closed container, protected from light. Store at -20°C or below under an inert atmosphere (e.g., argon or nitrogen) for long-term stability. This compound is strictly light-sensitive and should be handled under subdued light. Allow the container to reach ambient temperature before opening to minimize moisture condensation. Keep away from heat, sparks, and open flame.
Specification
| Item | Specification |
|---|---|
| Appearance | White to off-white solid |
| Identification (HPLC) | Retention time corresponds to reference standard |
| Identification (NMR) | Spectrum consistent with structure |
| Purity (HPLC) | ≥ 95.0% |
| Water Content (KF) | ≤ 1.0% |
| Residual Solvents (GC) | Complies with ICH Q3C guidelines |
Note: Specifications can be tailored. Please contact us for the detailed technical data sheet of a specific grade.
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