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CAS RN: 1024-99-3 | Product Number: I1154
5-Iodouridine
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Purity: >97.0%(HPLC)
Synonyms:
- 2,4-Dihydroxy-5-iodo-1-β-D-ribofuranosylpyrimidine
- 1-[(2R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl]-5-iodopyrimidine-2,4(1H,3H)-dione
Product Documents:
| Size | Unit Price | Hyderabad | Japan* | Quantity |
|---|---|---|---|---|
| 5G |
₹9,000.00
|
Contact Us | 29 |
|
*Upon orders receipt, Hyderabad stocks will be dispatched on the same day.
*Items available in Japan warehouse will be dispatched in 10-12 working days.
*INR price is exclusive of domestic taxes applicable.
*TCI frequently reviews storage conditions to optimize them. Please note that the latest information on the storage temperature for the products is described on our website.
| Product Number | I1154 |
| Purity / Analysis Method | >97.0%(HPLC) |
| Molecular Formula / Molecular Weight | C__9H__1__1IN__2O__6 = 370.10 |
| Physical State (20 deg.C) | Solid |
| Storage Temperature | Room Temperature (Recommended in a cool and dark place, <15°C) |
| Store Under Inert Gas | Store under inert gas |
| Condition to Avoid | Air Sensitive |
| CAS RN | 1024-99-3 |
| Reaxys Registry Number | 33665 |
| MDL Number | MFCD01114233 |
Specifications
| Appearance | White to Light yellow powder to crystal |
| Purity(HPLC) | min. 97.0 area% |
| Purity(Neutralization titration) | min. 98.0 % |
| Specific rotation | -21.0 ～ -25.0 deg(C=1, water) |
| NMR | confirm to structure |
Properties (reference)
| Melting Point | 204 °C |
GHS
Related Laws:
Transport Information:
Application
5-Iodouridine: A Starting Compound for the Synthesis of 5-Substituted Pyrimidine Nucleosides
5-Iodouridine, a pyrimidine nucleoside, is used as a starting compound for the synthesis of 5-substituted pyrimidine nucleosides, which has been shown to have biological properties such as antibacterial and antiviral activities.1-3) In addition, there are reported that 5-halogenated nucleosides, including 5-iodouridine, are incorporated into the DNA of replicating cells to facilitate DNA single-strand breaks and intra- or inter-strand crosslinks upon UV irradiation.4)
References
- 1) Synthesis and in vitro anti-mycobacterial activity of 5-substituted pyrimidine nucleosides
- 2) Synthesis and antiviral antiviral activity of (E)-5-(2-bromovinyl)uracil and (E)-5-(2-bromovinyl)uridine
- 3) Synthesis and in vitro antiviral activity of lipophilic pyrimidine nucleoside/carborane conjugates
- 4) Dehalogenation of Halogenated Nucleobases and Nucleosides by Organoselenium Compounds
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