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Catalog Number:
32114
CAS Number:
1272755-25-5
4-Methoxyphenyl 2-azido-3,6-di-O-benzyl-2-deoxy-β-D-glucopyranoside
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$72.31 /25MG
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Product Information

4-Methoxyphenyl 2-azido-3,6-di-O-benzyl-2-deoxy-b-D-glucopyranoside is a specialized compound with significant applications in the fields of medicinal chemistry and bioconjugation. This compound features a unique azido group, which makes it an excellent candidate for click chemistry, allowing for efficient and selective labeling of biomolecules. Its structure, characterized by the presence of methoxy and benzyl groups, enhances its solubility and stability, making it suitable for various synthetic pathways and biological applications. Researchers can utilize this compound in the development of targeted drug delivery systems and in the synthesis of glycosylated compounds, which are crucial for studying glycoprotein interactions and functions.

The versatility of 4-Methoxyphenyl 2-azido-3,6-di-O-benzyl-2-deoxy-b-D-glucopyranoside extends to its potential use in the synthesis of novel therapeutic agents and in the exploration of carbohydrate-based vaccines. Its ability to participate in bioorthogonal reactions opens up new avenues for the development of diagnostic tools and therapeutic strategies in cancer research and other diseases. With its unique properties and practical applications, this compound stands out as a valuable resource for researchers and industry professionals alike.

CAS Number
1272755-25-5
Molecular Formula
C27H29N3O6
Molecular Weight
491.54
MDL Number
MFCD08276393
PubChem ID
76030832
Appearance
White to off-white crystalline powder
Conditions
Store at ≤ -10 °C
General Information
CAS Number
1272755-25-5
Molecular Formula
C27H29N3O6
Molecular Weight
491.54
MDL Number
MFCD08276393
PubChem ID
76030832
Appearance
White to off-white crystalline powder
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

4-Methoxyphenyl 2-azido-3,6-di-O-benzyl-2-deoxy-b-D-glucopyranoside is widely utilized in research focused on:

  • Glycosylation Reactions: This compound serves as a glycosyl donor in synthetic chemistry, facilitating the formation of glycosidic bonds, which are crucial in the development of complex carbohydrates.
  • Drug Development: Its unique structure allows for modifications that can enhance the bioavailability and efficacy of pharmaceutical compounds, making it valuable in medicinal chemistry.
  • Bioconjugation: The azido group enables click chemistry applications, allowing researchers to attach this compound to various biomolecules for targeted drug delivery systems.
  • Diagnostics: It can be used in the development of diagnostic tools, particularly in the detection of specific biomolecules, due to its ability to form stable conjugates.
  • Material Science: The compound's properties make it suitable for creating functionalized materials, which can be applied in sensors and other advanced material applications.

Citations