3,4-Di-O-acetyl-6-deoxy-L-glucal
≥95%
- Product Code: 103706
CAS:
34819-86-8
| Molecular Weight: | 214.22 g./mol | Molecular Formula: | C₁₀H₁₄O₅ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00074970 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
Used in organic synthesis as a key intermediate for the preparation of various complex carbohydrates and glycoconjugates. It is particularly valuable in the synthesis of L-sugar derivatives, which are important in the development of pharmaceuticals and bioactive molecules. The acetyl groups protect the hydroxyl functionalities during chemical reactions, allowing for selective modifications. This compound is also employed in the study of glycosylation reactions, aiding in the understanding of enzymatic processes and the creation of novel glycosides. Its role in the development of antiviral and anticancer agents is significant, as it serves as a precursor for compounds with potential therapeutic properties. Additionally, it is utilized in carbohydrate chemistry research to explore new pathways for synthesizing rare sugars and their analogs.
Product Specification:
| Test | Specification |
|---|---|
| Appearance | Colorless To Yellow To Green Clear Liquid |
| Purity (%) | 94.5-100 |
| Infrared Spectrum | Conforms To Structure |
| Specific Rotation [a]20/D(Neat) | 61.0-+63.0 Degree Celsius |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.200 | 10-20 days | ฿1,180.00 |
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| 1.000 | 10-20 days | ฿5,390.00 |
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3,4-Di-O-acetyl-6-deoxy-L-glucal
Used in organic synthesis as a key intermediate for the preparation of various complex carbohydrates and glycoconjugates. It is particularly valuable in the synthesis of L-sugar derivatives, which are important in the development of pharmaceuticals and bioactive molecules. The acetyl groups protect the hydroxyl functionalities during chemical reactions, allowing for selective modifications. This compound is also employed in the study of glycosylation reactions, aiding in the understanding of enzymatic processes and the creation of novel glycosides. Its role in the development of antiviral and anticancer agents is significant, as it serves as a precursor for compounds with potential therapeutic properties. Additionally, it is utilized in carbohydrate chemistry research to explore new pathways for synthesizing rare sugars and their analogs.
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