The chemical substance known as 6-azido-6-deoxy-α-D-glucopyranoside, with the CAS number 18933-88-5, is a derivative of glucose characterized by the presence of an azido group (-N3) at the 6-position of the glucopyranose ring. This modification imparts unique properties, making it useful in various biochemical applications, particularly in the fields of glycoscience and bioconjugation. The azido group is notable for its reactivity in click chemistry, allowing for selective coupling with alkyne-containing molecules, which is valuable in the synthesis of complex biomolecules and materials. The compound typically exists as a white to off-white solid and is soluble in polar solvents. Its structure retains the typical pyranose ring conformation, which is crucial for its biological interactions. As a 6-deoxy derivative, it lacks a hydroxyl group at the 6-position, further influencing its reactivity and potential applications in drug development and molecular biology. Safety and handling precautions should be observed due to the reactive nature of the azido group.

a-D-Glucopyranoside,6-azido-6-deoxy-a-D-glucopyranosyl6-azido-6-deoxy-

18933-88-5: The chemical substance known as 6-azido-6-deoxy-α-D-glucopyranoside, with the CAS number 18933-88-5, is a derivative of glucose characterized by the presence of an azido group (-N3) at the 6-position of the glucopyranose ring. This modification imparts unique properties, making it useful in various biochemical applications, particularly in the fields of glycoscience and bioconjugation. The azido group is notable for its reactivity in click chemistry, allowing for selective coupling with alkyne-containing molecules, which is valuable in the synthesis of complex biomolecules and materials. The compound typically exists as a white to off-white solid and is soluble in polar solvents. Its structure retains the typical pyranose ring conformation, which is crucial for its biological interactions. As a 6-deoxy derivative, it lacks a hydroxyl group at the 6-position, further influencing its reactivity and potential applications in drug development and molecular biology. Safety and handling precautions should be observed due to the reactive nature of the azido group.

6,6'-Diazido-6,6'-dideoxytrehalose

6,6'-Diazido-6,6'-dideoxy-α,α-D-trehalose

CAS 18933-88-5

a-D-Glucopyranoside,6-azido-6-deoxy-a-D-glucopyranosyl6-azido-6-deoxy-

6,6'-Diazido-6,6'-dideoxytrehalose

Ref: 3B-D5372

6,6'-Diazido-6,6'-dideoxy-α,α-D-trehalose

Ref: 54-BICL4068

6,6''-Diazido-6,6''-dideoxy-α,α-D-trehalose

Ref: 7W-GC2126