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Catalog Number:
32249
CAS Number:
79528-48-6
Methyl 3,4,6-tri-O-acetyl-2-deoxy-2-phthalimido-1-thio-ॆ-D-glucopyranoside
Purity:
≥ 98% (HPLC, T)
Documents
$72.31 /100MG
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Product Information

Methyl 3,4,6-tri-O-acetyl-2-deoxy-2-phthalimido-1-thio-b-D-glucopyranoside is a specialized compound that plays a significant role in the synthesis of glycosides and other carbohydrate derivatives. This compound is particularly valuable in pharmaceutical research and development, where it is utilized as a building block for the creation of various bioactive molecules. Its unique structure, featuring multiple acetyl groups and a phthalimido moiety, enhances its reactivity and solubility, making it an ideal candidate for glycosylation reactions.

In addition to its applications in synthetic organic chemistry, this compound is also explored for its potential in drug formulation and delivery systems. Researchers appreciate its ability to modify the pharmacokinetic properties of therapeutic agents, thereby improving their efficacy and bioavailability. With its versatile applications in both academic and industrial settings, Methyl 3,4,6-tri-O-acetyl-2-deoxy-2-phthalimido-1-thio-b-D-glucopyranoside stands out as a crucial tool for advancing glycoscience and medicinal chemistry.

CAS Number
79528-48-6
Purity
≥ 98% (HPLC, T)
Molecular Formula
C21H23NO9S
Molecular Weight
465.47
MDL Number
MFCD00080802
PubChem ID
13991661
Melting Point
148-152° C
Appearance
White to off-white crystalline powder
Optical Rotation
[a]20/D= +48 to +51° (C=1 in CHCl3
Conditions
Store at ≤ -10 °C
General Information
CAS Number
79528-48-6
Purity
≥ 98% (HPLC, T)
Molecular Formula
C21H23NO9S
Molecular Weight
465.47
MDL Number
MFCD00080802
PubChem ID
13991661
Melting Point
148-152° C
Appearance
White to off-white crystalline powder
Optical Rotation
[a]20/D= +48 to +51° (C=1 in CHCl3
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

Methyl 3,4,6-tri-O-acetyl-2-deoxy-2-phthalimido-1-thio-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 in carbohydrate synthesis, which is crucial for developing new drugs and biomolecules.
  • Antibody Development: It is used in the preparation of glycoproteins for antibody production, enhancing the immunogenicity of therapeutic proteins, which is vital in vaccine development and cancer therapies.
  • Drug Delivery Systems: The compound can be incorporated into drug delivery systems, improving the solubility and bioavailability of poorly soluble drugs, thus enhancing their therapeutic effectiveness.
  • Bioconjugation: It plays a significant role in bioconjugation techniques, allowing researchers to attach biomolecules to surfaces or other molecules, which is essential in diagnostics and targeted therapies.
  • Research in Enzyme Inhibition: This chemical is studied for its potential to inhibit specific enzymes, providing insights into metabolic pathways and aiding in the design of enzyme inhibitors for therapeutic applications.

Citations