1,2,4,6-Tetra-O-acetyl-3-O-allyl-β-D-glucopyranose
≥98%
- Product Code: 103614
CAS:
39698-00-5
Molecular Weight: | 388.37 g./mol | Molecular Formula: | C₁₇H₂₄O₁₀ |
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EC Number: | MDL Number: | ||
Melting Point: | 117-121°C | Boiling Point: | |
Density: | Storage Condition: | -20°C |
Product Description:
This chemical is primarily used in organic synthesis as an intermediate for the preparation of more complex carbohydrate derivatives. It serves as a key building block in the development of glycosides, which are important in the study of glycobiology and the synthesis of bioactive molecules. Its acetyl and allyl groups provide protection for specific hydroxyl sites, allowing selective reactions to occur during the synthesis process. This compound is also utilized in the production of glycoconjugates, which have applications in drug development, vaccine design, and the study of cellular communication. Additionally, it plays a role in the creation of modified sugars for use in research on enzyme mechanisms and metabolic pathways.
Product Specification:
Test | Specification |
---|---|
Appearance | White - Almost White Crystal - Powder |
Purity (%) | 97.5-100 |
Specific Rotation [A]20/D(C=1, CHCl3) | -4.0--1.0 |
Infrared Spectrum | Conforms To Structure |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.250 | 10-20 days | ฿4,221.00 |
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1,2,4,6-Tetra-O-acetyl-3-O-allyl-β-D-glucopyranose
This chemical is primarily used in organic synthesis as an intermediate for the preparation of more complex carbohydrate derivatives. It serves as a key building block in the development of glycosides, which are important in the study of glycobiology and the synthesis of bioactive molecules. Its acetyl and allyl groups provide protection for specific hydroxyl sites, allowing selective reactions to occur during the synthesis process. This compound is also utilized in the production of glycoconjugates, which have applications in drug development, vaccine design, and the study of cellular communication. Additionally, it plays a role in the creation of modified sugars for use in research on enzyme mechanisms and metabolic pathways.
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