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Catalog Number:
27953
CAS Number:
14131-84-1
2,3,5,6-Di-O-isopropylidene-ॅ-D-mannofuranose
Purity:
≥ 98% (assay)
Synonym(s):
D-Mannose diacetonide
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Product Information

2,3,5,6-Di-O-isopropylidene-α-D-mannofuranose is a versatile carbohydrate derivative that plays a significant role in various fields, including organic synthesis and medicinal chemistry. This compound is particularly valued for its ability to serve as a protecting group for hydroxyl functionalities in carbohydrate chemistry, facilitating the synthesis of more complex molecules. Its unique structure allows for selective reactions, making it an essential tool for researchers working on glycosylation reactions and the development of glycosides.

In addition to its synthetic applications, 2,3,5,6-Di-O-isopropylidene-α-D-mannofuranose is also utilized in the formulation of pharmaceuticals and nutraceuticals, where it can enhance the stability and bioavailability of active ingredients. Its favorable properties, such as solubility and reactivity, make it an attractive choice for professionals looking to optimize their formulations. With its broad range of applications, this compound is indispensable for researchers and industry professionals aiming to innovate in carbohydrate chemistry and related fields.

Synonyms
D-Mannose diacetonide
CAS Number
14131-84-1
Purity
≥ 98% (assay)
Molecular Formula
C12H20O6
Molecular Weight
260.28
MDL Number
MFCD00134206
PubChem ID
230386
Melting Point
120-126 °C
Appearance
White to almost white crystalline powder
Conditions
Store at 0-8°C
General Information
Synonyms
D-Mannose diacetonide
CAS Number
14131-84-1
Purity
≥ 98% (assay)
Molecular Formula
C12H20O6
Molecular Weight
260.28
MDL Number
MFCD00134206
PubChem ID
230386
Melting Point
120-126 °C
Appearance
White to almost white crystalline powder
Conditions
Store at 0-8°C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

2,3,5,6-Di-O-isopropylidene-a-D-mannofuranose is widely utilized in research focused on:

  • Carbohydrate Chemistry: This compound serves as a key intermediate in the synthesis of various carbohydrate derivatives, enabling researchers to explore new glycosylation reactions and carbohydrate-based materials.
  • Drug Development: It is used in the design of glycosylated drugs, which can enhance the bioavailability and efficacy of therapeutic agents, particularly in targeting specific biological pathways.
  • Biotechnology: The compound plays a role in the development of glycoproteins and polysaccharides, which are crucial for vaccine formulation and other biopharmaceutical applications.
  • Food Industry: It can be utilized in the formulation of food additives that mimic natural sugars, providing sweetness without the caloric content, appealing to health-conscious consumers.
  • Research on Glycobiology: This compound aids in the study of carbohydrate-protein interactions, which are vital for understanding various biological processes, including cell signaling and immune responses.

Citations