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Catalog Number:
32229
CAS Number:
86520-63-0
2,3,4,6-Tetra-O-acetyl-ॅ-D-galactopyranosyl 2,2,2-trichloroacetimidate
Purity:
≥ 98% (HPLC)
Documents
$86.23 /250MG
Pack Size Availability Price
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Product Information

2,3,4,6-Tetra-O-acetyl-a-D-galactopyranosyl 2,2,2-trichloroacetimidate is a versatile glycosyl donor widely utilized in carbohydrate chemistry for the synthesis of complex oligosaccharides and glycoconjugates. This compound is particularly valued for its ability to facilitate glycosidic bond formation, making it essential in the development of glycosylated pharmaceuticals and biologically active compounds. Its unique structure, featuring multiple acetyl groups, enhances its stability and reactivity, allowing for efficient coupling reactions under mild conditions.

Researchers and industry professionals can leverage this compound in various applications, including the synthesis of glycoproteins, glycolipids, and other carbohydrate-based materials. Its use in the pharmaceutical industry is noteworthy, as it aids in the design of drug candidates with improved efficacy and bioavailability. Additionally, the compound's compatibility with diverse reaction conditions makes it an attractive choice for synthetic chemists aiming to streamline their processes while achieving high yields.

CAS Number
86520-63-0
Purity
≥ 98% (HPLC)
Molecular Formula
C16H20Cl3NO10
Molecular Weight
492.68
MDL Number
MFCD07369652
PubChem ID
5201201
Melting Point
120-124° C
Appearance
Light yellow crystalline powder
Optical Rotation
[a]20/D= +109 to +115° (C=1 in CHCl3
Conditions
Store at ≤ -10 °C
General Information
CAS Number
86520-63-0
Purity
≥ 98% (HPLC)
Molecular Formula
C16H20Cl3NO10
Molecular Weight
492.68
MDL Number
MFCD07369652
PubChem ID
5201201
Melting Point
120-124° C
Appearance
Light yellow crystalline powder
Optical Rotation
[a]20/D= +109 to +115° (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

2,3,4,6-Tetra-O-acetyl-a-D-galactopyranosyl 2,2,2-trichloroacetimidate is widely utilized in research focused on:

  • Synthetic Carbohydrate Chemistry: This compound serves as a key intermediate in the synthesis of complex carbohydrates, enabling researchers to create glycosylated compounds for various applications.
  • Drug Development: It plays a crucial role in the development of glycosylated drugs, which can enhance the bioavailability and efficacy of therapeutic agents, particularly in the treatment of infectious diseases.
  • Vaccine Formulation: The compound is used in the design of carbohydrate-based vaccines, which can stimulate a stronger immune response, providing better protection against pathogens.
  • Biotechnology: In the field of biotechnology, it is employed to modify proteins and enzymes, improving their stability and functionality for industrial applications.
  • Research in Glycobiology: This chemical is essential for studying the structure and function of glycoproteins and glycolipids, contributing to advancements in understanding cellular interactions and disease mechanisms.

Citations