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Catalog Number:
32253
CAS Number:
10022-13-6
1,3,4,6-Tetra-O-acetyl-2-deoxy-2-phthalimido-ॆ-D-glucopyranose
Purity:
≥ 98% (HPLC)
Documents
$18.53 /1G
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Product Information

1,3,4,6-Tetra-O-acetyl-2-deoxy-2-phthalimido-β-D-glucopyranose is a versatile compound widely utilized in the synthesis of glycosylated molecules and as a protective group in carbohydrate chemistry. This compound is particularly valuable for researchers focusing on the development of glycosides, which are essential in various biological processes and pharmaceutical applications. Its unique structure allows for selective reactions, making it an ideal choice for chemists looking to streamline their synthetic pathways while maintaining high yields.

In addition to its role in organic synthesis, this compound is also significant in the field of medicinal chemistry, where it can be employed in the design of novel drug candidates. Its acetyl groups provide stability and solubility, enhancing the bioavailability of the resulting compounds. Researchers have successfully used 1,3,4,6-Tetra-O-acetyl-2-deoxy-2-phthalimido-β-D-glucopyranose in the development of targeted therapies and diagnostic agents, showcasing its potential in advancing healthcare solutions.

CAS Number
10022-13-6
Purity
≥ 98% (HPLC)
Molecular Formula
C22H23NO11
Molecular Weight
477.42
MDL Number
MFCD00080781
PubChem ID
3791025
Melting Point
200° C
Appearance
White to light yellow crystalline powder
Optical Rotation
[a]20/D= +66 to +70° (C=1 in CHCl3
Conditions
Store at ≤ -10 °C
General Information
CAS Number
10022-13-6
Purity
≥ 98% (HPLC)
Molecular Formula
C22H23NO11
Molecular Weight
477.42
MDL Number
MFCD00080781
PubChem ID
3791025
Melting Point
200° C
Appearance
White to light yellow crystalline powder
Optical Rotation
[a]20/D= +66 to +70° (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

1,3,4,6-Tetra-O-acetyl-2-deoxy-2-phthalimido-b-D-glucopyranose is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a key intermediate in the synthesis of various glycosylated drugs, enhancing their bioavailability and therapeutic efficacy.
  • Biotechnology: It is employed in the development of glycoproteins and other biomolecules, playing a crucial role in vaccine formulation and antibody production.
  • Carbohydrate Chemistry: Researchers use it to study carbohydrate interactions and modifications, aiding in the understanding of glycosylation processes.
  • Food Industry: The compound can be utilized as a food additive for enhancing flavor profiles and preserving freshness, particularly in specialty products.
  • Diagnostic Applications: It is involved in the creation of specific assays and tests, improving the accuracy of disease detection and monitoring through glycan analysis.

Citations