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Catalog Number:
32205
CAS Number:
889453-83-2
4-Methoxyphenyl 3-O-allyl-2-azido-4,6-O-benzylidene-2-deoxy-β-D-galactopyranoside
Purity:
≥ 98% (HPLC)
Documents
$100.05 /25MG
Pack Size Availability Price
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Product Information

4-Methoxyphenyl 3-O-allyl-2-azido-4,6-O-benzylidene-2-deoxy-b-D-galactopyranoside is a versatile compound with significant applications in the fields of medicinal chemistry and biochemistry. This compound, characterized by its unique azido and benzylidene functionalities, serves as a valuable intermediate in the synthesis of glycosylated compounds, which are essential in drug development and carbohydrate chemistry. Its ability to undergo click chemistry reactions makes it particularly useful for bioconjugation and the development of targeted drug delivery systems.

Researchers appreciate this compound for its stability and reactivity, allowing for the efficient formation of glycosidic bonds. Its methoxy and allyl groups enhance its solubility and reactivity, making it suitable for various organic transformations. Additionally, the compound's structural features enable its use in the synthesis of glycoproteins and other biologically relevant molecules, paving the way for advancements in therapeutic agents and diagnostic tools.

CAS Number
889453-83-2
Purity
≥ 98% (HPLC)
Molecular Formula
C23H25N3O6
Molecular Weight
439.47
MDL Number
MFCD09038531
PubChem ID
75059406
Appearance
White to off-white crystalline powder
Conditions
Store at ≤ -10 °C
General Information
CAS Number
889453-83-2
Purity
≥ 98% (HPLC)
Molecular Formula
C23H25N3O6
Molecular Weight
439.47
MDL Number
MFCD09038531
PubChem ID
75059406
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 3-O-allyl-2-azido-4,6-O-benzylidene-2-deoxy-b-D-galactopyranoside is widely utilized in research focused on:

  • Glycosylation Reactions: This compound serves as a versatile glycosyl donor in synthetic chemistry, facilitating the formation of glycosidic bonds in the creation of complex carbohydrates.
  • Drug Development: Its unique structure allows for modifications that can lead to the development of novel pharmaceuticals, particularly in targeting specific biological pathways.
  • Bioconjugation: The azido group enables click chemistry applications, making it ideal for attaching biomolecules to surfaces or other compounds in biotechnological applications.
  • Research in Carbohydrate Chemistry: This compound is instrumental in studying carbohydrate interactions and functions, aiding researchers in understanding biological processes at the molecular level.
  • Material Science: It can be used in the synthesis of functionalized polymers, enhancing material properties for applications in coatings, adhesives, and drug delivery systems.

Citations