D-Fructose, 5-azido-5-deoxy- is a modified sugar derivative of fructose, characterized by the presence of an azido group (-N3) at the 5-position of the sugar molecule. This modification imparts unique chemical properties, making it useful in various biochemical applications, particularly in the fields of glycoscience and bioconjugation. The azido group is known for its reactivity in click chemistry, allowing for selective labeling and attachment to other biomolecules. D-Fructose itself is a naturally occurring ketohexose, and the introduction of the azido group alters its reactivity and solubility. The compound is typically a white to off-white solid and is soluble in water, which is a common characteristic of many sugars. Its molecular structure allows it to participate in various chemical reactions, making it a valuable tool in synthetic organic chemistry and biochemistry. Safety data and handling precautions should be observed due to the potential hazards associated with azido compounds.

D-Fructose,5-azido-5-deoxy-

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Applications 5-Azido-5-deoxy-D-fructose (cas# 94801-02-2) is a compound useful in organic synthesis.


5-Azido-5-deoxy-D-fructose

5-Azido-5-deoxy-D-fructose is a chiral compound that has been synthesized by the catalytic hydrogenation of 5-azido-4,6-dideoxy-D-glucose. The kinetic and stereoselective synthesis of 5-azido-5-deoxy-D-fructose is achieved by using an acetylating agent to first generate the corresponding acetic acid derivative. The enantiomeric excess in this reaction was 88%. This compound can be used as a precursor for the synthesis of polyhydroxylated compounds, such as 3,4,5,6 tetrahydroxybenzoate.

CAS 94801-02-2: D-Fructose,5-azido-5-deoxy-

5-Azido-5-deoxy-D-fructose

Ref: TR-A824200

5-Azido-5-deoxy-D-fructose

Ref: 3D-MA04534

D-Fructose, 5-azido-5-deoxy-

Ref: IN-DA01CBY2

5-Azido-5-deoxy-D-fructose

Ref: 7W-GC0401