Search Thermo Fisher Scientific
Element Search
Structure Search
Thermo Scientific Chemicals
2'-Fluoro-2'-deoxyuridine, 97%
Have Questions?
Change view
Catalog number J65948.03
also known as J65948-03
Price (USD)/ Each
33.50
-
Quantity:
1 g
Price (USD)/ Each
33.50
2'-Fluoro-2'-deoxyuridine, 97%
Catalog numberJ65948.03
Price (USD)/ Each
33.50
-
Chemical Identifiers
CAS784-71-4
IUPAC Name1-[(2R,3R,4R,5R)-3-fluoro-4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]-1,2,3,4-tetrahydropyrimidine-2,4-dione
Molecular FormulaC9H11FN2O5
InChI KeyUIYWFOZZIZEEKJ-XVFCMESISA-N
SMILESOC[C@H]1O[C@H]([C@H](F)[C@@H]1O)N1C=CC(=O)NC1=O
View more
Specifications
Specification Sheet
Specification SheetAssay from Supplier's CofA≥96.0%
FormPowder or crystals or crystalline powder
Appearance (Color)White to off-white
2'-Fluoro-2'-deoxyuridine is used as a component incorporated into therapeutic oligonucleotides to combat prostate and breast cancer.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Applications
2′-Fluoro-2′-deoxyuridine is used as a component incorporated into therapeutic oligonucleotides to combat prostate and breast cancer.
Solubility
Soluble in methanol.
Notes
Store in cool, dry conditions in well sealed containers. Keep container tightly closed.
2′-Fluoro-2′-deoxyuridine is used as a component incorporated into therapeutic oligonucleotides to combat prostate and breast cancer.
Solubility
Soluble in methanol.
Notes
Store in cool, dry conditions in well sealed containers. Keep container tightly closed.
RUO – Research Use Only
General References:
- Charles L. Perrin. Mechanism of hydrogen exchange in amides. J. Am. Chem. Soc. 1974, 96, (17), 5628-5631.
- Osamu Shimomura; Ikuyoshi Tomita; Takeshi Endo. Cationic polymerization of glycidyl phenyl ether initiated by various arylsulfoniu∼ salts as new thermal latent cationic initiators. Macromol. Rapid Cammun. 1998, 19 (9), 493-497 .