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Catalog Number:
32280
CAS Number:
13350-45-3
Methyl 2,3,4,6-tetra-O-acetyl-1-thio-β-D-glucopyranoside
Purity:
≥ 98% (GC)
Documents
$93.14 /250MG
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Product Information

Methyl 2,3,4,6-tetra-O-acetyl-1-thio-b-D-glucopyranoside is a versatile thio-glycoside compound that plays a significant role in carbohydrate chemistry and glycosylation reactions. This compound is particularly valued for its ability to serve as a glycosyl donor in the synthesis of complex carbohydrates and glycoconjugates, making it an essential tool for researchers in the fields of biochemistry and medicinal chemistry. Its unique structure, featuring multiple acetyl groups, enhances its stability and reactivity, allowing for efficient coupling reactions that are crucial in the development of glycosylated pharmaceuticals and biologically active compounds.

In addition to its applications in synthetic chemistry, Methyl 2,3,4,6-tetra-O-acetyl-1-thio-b-D-glucopyranoside is also utilized in the study of carbohydrate-protein interactions, which are fundamental to understanding various biological processes. Researchers can leverage this compound to explore the roles of glycosylation in cell signaling and immune responses, providing insights that could lead to novel therapeutic strategies. Its favorable properties and broad applicability make it a valuable asset for both academic and industrial laboratories focused on carbohydrate research and development.

CAS Number
13350-45-3
Purity
≥ 98% (GC)
Molecular Formula
C15H22O9S
Molecular Weight
378.39
MDL Number
MFCD00080807
PubChem ID
4601087
Appearance
White to off-white crystalline powder
Optical Rotation
[a]20/D= -13 to -17° (C=1 in CHCl3
Conditions
Store at 2-8 °C
General Information
CAS Number
13350-45-3
Purity
≥ 98% (GC)
Molecular Formula
C15H22O9S
Molecular Weight
378.39
MDL Number
MFCD00080807
PubChem ID
4601087
Appearance
White to off-white crystalline powder
Optical Rotation
[a]20/D= -13 to -17° (C=1 in CHCl3
Conditions
Store at 2-8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Methyl 2,3,4,6-tetra-O-acetyl-1-thio-b-D-glucopyranoside is widely utilized in research focused on:

  • Glycosylation Reactions: This compound serves as a glycosyl donor in synthetic chemistry, enabling the formation of glycosidic bonds in the production of complex carbohydrates.
  • Drug Development: It is used in the synthesis of glycosylated drugs, enhancing their bioavailability and stability, which is crucial in pharmaceutical formulations.
  • Biochemical Research: Researchers employ it to study carbohydrate-protein interactions, aiding in the understanding of cellular processes and disease mechanisms.
  • Food Industry: The compound can be applied in flavoring and sweetening agents, providing a natural alternative to synthetic additives.
  • Diagnostics: It plays a role in the development of diagnostic tools, particularly in assays that require specific carbohydrate recognition elements.

Citations