CAS 252337-58-9
:Uridine,2'-deoxy-5-[3-oxo-3-[[6-[(trifluoroacetyl)amino]hexyl]amino]-1-propenyl]- (9CI)
Description:
Uridine, 2'-deoxy-5-[3-oxo-3-[[6-[(trifluoroacetyl)amino]hexyl]amino]-1-propenyl]- (9CI), with the CAS number 252337-58-9, is a synthetic nucleoside derivative that features a modified uridine structure. This compound is characterized by the presence of a 2'-deoxy ribose sugar, which distinguishes it from standard uridine. The molecule contains a propenyl side chain that is further substituted with a hexyl chain linked to a trifluoroacetyl group, contributing to its unique chemical properties. The trifluoroacetyl moiety enhances the lipophilicity and stability of the compound, making it potentially useful in various biochemical applications. Its structural modifications may influence its interaction with biological targets, such as nucleic acids or proteins, and could be of interest in drug development or molecular biology research. As with many synthetic compounds, its solubility, stability, and reactivity will depend on the specific conditions under which it is studied. Safety and handling precautions should be observed due to the presence of trifluoroacetyl groups, which can be hazardous.
Formula:C20H27F3N4O7
Synonyms:- 5-[N-(6-(Trifluoroacetamido)Hexyl)-3(E)-Acrylamido]-2’-Deoxyuridine
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 2 products.
5-[N(6-(Trifluoroacetamido)hexyl)-3-(E)-acrylamido] -2'-deoxyuridine
CAS:<p>5-[N(6-(Trifluoroacetamido)hexyl)-3-(E)-acrylamido] -2'-deoxyuridine is a synthetic, modified nucleoside that functions as an activator of ribonucleotide reductase. It has been shown to be effective in the treatment of viral infections, including herpes simplex virus type 1 (HSV-1), herpes simplex virus type 2 (HSV-2), and human immunodeficiency virus type 1 (HIV-1). 5-[N(6-(Trifluoroacetamido)hexyl)-3-(E)-acrylamido] -2'-deoxyuridine is also synthesized into DNA or RNA molecules, which are used to study the structure of these compounds. It can also be used for phosphoramidite synthesis.</p>Formula:C20H27F3N4OPurity:Min. 95%Molecular weight:396.45 g/mol

