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Catalog Number:
32244
CAS Number:
1430068-18-0
4-Metoxifenil 2-azido-4,6- O -bencilideno-2-desoxi-β-D-glucopiranósido
Purity:
≥ 98 % (HPLC)
Documents
$93.14 /100 mg
Tamaño
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Product Information

Conservar lejos de agentes oxidantes y fuentes de ignición.

CAS Number
1430068-18-0
Purity
≥ 98 % (HPLC)
Molecular Formula
C20H21N3O6
Molecular Weight
399.4
MDL Number
MFCD06797146
PubChem ID
75059405
Melting Point
160-165? C
Appearance
Polvo cristalino de color blanco a blanquecino.
Optical Rotation
[a]20/D= -3 a -6° (C=1 en CHCl 3 )
Conditions
Conservar a ≤ -10 °C
General Information
CAS Number
1430068-18-0
Purity
≥ 98 % (HPLC)
Molecular Formula
C20H21N3O6
Molecular Weight
399.4
MDL Number
MFCD06797146
PubChem ID
75059405
Melting Point
160-165? C
Appearance
Polvo cristalino de color blanco a blanquecino.
Optical Rotation
[a]20/D= -3 a -6° (C=1 en CHCl 3 )
Conditions
Conservar a ≤ -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-4,6-O-benzylidene-2-deoxy-b-D-glucopyranoside is widely utilized in research focused on:

  • Bioconjugation: This compound serves as a versatile linker in bioconjugation processes, allowing researchers to attach biomolecules to surfaces or other molecules, enhancing the development of targeted drug delivery systems.
  • Medicinal Chemistry: It is employed in the synthesis of novel glycosylated compounds, which can lead to the discovery of new therapeutic agents, particularly in the treatment of infectious diseases.
  • Diagnostics: The azido group in the compound can be used in click chemistry, facilitating the development of diagnostic tools that can rapidly identify specific biomolecules in clinical samples.
  • Material Science: This chemical can be incorporated into polymer matrices to create smart materials with specific functionalities, such as responsive drug release or enhanced mechanical properties.
  • Research on Glycobiology: It plays a crucial role in studying carbohydrate-protein interactions, helping researchers understand biological processes and develop new strategies for disease intervention.

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