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Catalog Number:
32233
CAS Number:
168397-51-1
2-Acetamido-4,6-O-benzylidene-2-deoxy-β-D-glucopyranosyl azide
Purity:
≥ 98% (HPLC)
Documents
$65.40 /100MG
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Product Information

2-Acetamido-4,6-O-benzylidene-2-deoxy-b-D-glucopyranosyl azide is a specialized chemical compound that plays a significant role in carbohydrate chemistry and bioconjugation applications. This compound is recognized for its unique azide functional group, which allows for efficient click chemistry reactions, making it an invaluable tool for researchers in the fields of medicinal chemistry and materials science. Its structure, featuring a glucopyranosyl moiety, enhances its compatibility with biological systems, facilitating the development of glycosylated drugs and biomolecules.

The versatility of 2-Acetamido-4,6-O-benzylidene-2-deoxy-b-D-glucopyranosyl azide extends to its use in synthesizing glycoproteins and glyconjugates, which are crucial for vaccine development and targeted drug delivery systems. Additionally, its ability to participate in selective reactions opens avenues for creating novel biomaterials with tailored properties. Researchers can leverage this compound to explore innovative solutions in drug design, diagnostics, and therapeutic applications, making it a valuable addition to any laboratory focused on cutting-edge chemical research.

CAS Number
168397-51-1
Purity
≥ 98% (HPLC)
Molecular Formula
C15H18N4O5
Molecular Weight
334.33
MDL Number
MFCD07778221
PubChem ID
5211194
Appearance
White to off-white crystalline powder
Optical Rotation
[a]20/D= -95 to -99° (C=0.5 in MeOH)
Conditions
Store at ≤ -10 °C
General Information
CAS Number
168397-51-1
Purity
≥ 98% (HPLC)
Molecular Formula
C15H18N4O5
Molecular Weight
334.33
MDL Number
MFCD07778221
PubChem ID
5211194
Appearance
White to off-white crystalline powder
Optical Rotation
[a]20/D= -95 to -99° (C=0.5 in MeOH)
Conditions
Store at ≤ -10 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

2-Acetamido-4,6-O-benzylidene-2-deoxy-b-D-glucopyranosyl azide is widely utilized in research focused on:

  • Glycosylation Reactions: This compound serves as a glycosyl donor in synthetic chemistry, facilitating the creation of complex carbohydrates, which are essential in drug development and vaccine formulation.
  • Bioconjugation: It is employed in bioconjugation processes, allowing researchers to attach biomolecules to surfaces or other molecules, enhancing the functionality of therapeutic agents and diagnostic tools.
  • Drug Development: The compound plays a role in the synthesis of glycosylated drugs, improving their stability and bioavailability, which is crucial for effective treatment options in pharmaceuticals.
  • Research in Glycobiology: It aids in the study of glycan structures and their interactions, providing insights into cellular processes and disease mechanisms, particularly in cancer and infectious diseases.
  • Material Science: This chemical is used in the development of glyco-materials, which have applications in biosensors and targeted drug delivery systems, offering innovative solutions in medical technology.

Citations