
CAS 15379-29-0
:5-fluoro-1-[(2S,5R)-5-(hydroxymethyl)-2,5-dihydrofuran-2-yl]pyrimidine-2,4-dione
Description:
5-Fluoro-1-[(2S,5R)-5-(hydroxymethyl)-2,5-dihydrofuran-2-yl]pyrimidine-2,4-dione, with the CAS number 15379-29-0, is a synthetic organic compound characterized by its pyrimidine core and a fluorine substituent. This compound features a hydroxymethyl group attached to a dihydrofuran ring, contributing to its structural complexity and potential biological activity. The presence of the fluorine atom can enhance the compound's lipophilicity and metabolic stability, making it of interest in medicinal chemistry, particularly in the development of pharmaceuticals. The stereochemistry indicated by the (2S,5R) configuration suggests specific spatial arrangements that may influence the compound's interactions with biological targets. As a pyrimidine derivative, it may exhibit properties typical of nucleobases, such as involvement in nucleic acid metabolism or inhibition of enzymes. Overall, this compound's unique structure and functional groups suggest potential applications in drug development and research in biochemistry.
Formula:C9H9FN2O4
InChI:InChI=1/C9H9FN2O4/c10-6-3-12(9(15)11-8(6)14)7-2-1-5(4-13)16-7/h1-3,5,7,13H,4H2,(H,11,14,15)/t5-,7+/m1/s1
Synonyms:- 2,4(1H,3H)-pyrimidinedione, 1-[(2S,5R)-2,5-dihydro-5-(hydroxymethyl)-2-furanyl]-5-fluoro-
- 5-fluoro-1-[(2S,5R)-5-(hydroxymethyl)-2,5-dihydrofuran-2-yl]pyrimidine-2,4(1H,3H)-dione
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Found 2 products.
2',3'-Dideoxy-2',3'-didehydro-5-fluoro-uridine
CAS:<p>2',3'-Dideoxy-2',3'-didehydro-5-fluoro-uridine is a Nucleoside Derivative - Didehydro-nucleoside; Fluoro-modified nucleoside.</p>Formula:C9H9FN2O4Color and Shape:SolidMolecular weight:228.182',3'-Dideoxy-2',3'-didehydro-5-fluoro-uridine,
CAS:<p>2',3'-Dideoxy-2',3'-didehydro-5-fluoro-uridine is a nucleoside that is used as an antiviral agent. This drug has been shown to inhibit the replication of HIV in vitro and in vivo. It has also been shown to be nontoxic and well tolerated in humans, with no adverse effects on white blood cell counts, liver function, or kidney function. The mechanism of action of 2',3'-dideoxy-2',3'-didehydro-5-fluoro-uridine is not known. It may inhibit viral DNA synthesis by blocking the incorporation of uracil into DNA or by inhibiting the activity of RNA polymerase.</p>Formula:C9H9FN2O4Purity:Min. 95%Molecular weight:228.18 g/mol

