CAS 444586-86-1
:D-Arabinofuranose,2-deoxy-2-fluoro-, triacetate (9CI)
Description:
D-Arabinofuranose, 2-deoxy-2-fluoro-, triacetate (9CI) is a synthetic derivative of the naturally occurring sugar arabinose, modified to include a fluorine atom at the 2-position and acetyl groups at the hydroxyl positions. This compound is characterized by its molecular structure, which features a furanose ring, a five-membered cyclic form of sugar, and the presence of three acetyl groups that enhance its lipophilicity and stability. The introduction of the fluorine atom can influence the compound's biological activity, potentially affecting its interaction with enzymes and receptors. D-Arabinofuranose derivatives are often studied for their applications in medicinal chemistry, particularly in the development of antiviral and anticancer agents. The triacetate form suggests that the compound is likely to be more soluble in organic solvents, making it suitable for various chemical reactions and biological assays. As with many sugar derivatives, it may exhibit specific stereochemical properties that are crucial for its biological function and reactivity.
Formula:C11H15FO7
Synonyms:- 2-Fluoro-2-Deoxy-1,3,5-Tri-O-Acetyl-A-D-Arabinofuranosediscontinued
- 2-Fluoro-2-deoxy-1,3,5-tri-O-acetyl-alpha-D-arabinofuranose
- 2-Fluoro-2-deoxy-1,3,5-tri-O-acetyl-a-D-arabinofuranose
- 1,3,5-Tri-O-acetyl-2-deoxy-2-fluoro-a-D-arabinofuranose
- 2-Fluoro-2-deoxy-1,3,5-tri-O-acetyl-a-arabinofuranose
- Discontinued
- D-Arabinofuranose,2-deoxy-2-fluoro-, triacetate (9CI)
- acetic acid (3,5-diacetyloxy-4-fluoro-2-oxolanyl)methyl ester
- 2-FLUORO-2-DEOXY-1,3,5-TRI-O-ACETYL-A-D-ARABINOFURANOSEDISCONTINUED USP/EP/BP
- 2-Deoxy-2-fluoro-D-arabinofuranose triacetate
- 2-Fluoro-2-deoxy-1,3,5-tri-O-acetyl-α-D-arabinofuranose Discontinued
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 2 products.
1,3,5-Tri-O-acetyl-2-deoxy-2-fluoro-a-D-arabinofuranose
CAS:1,3,5-Tri-O-acetyl-2-deoxy-2-fluoro-a-D-arabinofuranose is a sugar that is modified with fluorine. It has been synthesized using the "click" reaction methodology and is available for custom synthesis. This synthetic sugar can be used in glycosylation reactions or as a monosaccharide or polysaccharide in complex carbohydrate click chemistry. This product is of high purity and can be modified with methyl groups or other functional groups to suit your needs.Formula:C11H15FO7Purity:Min. 95%Molecular weight:278.23 g/molRef: 3D-MT04737
Discontinued product

