1,2,3,4-Tetra-O-acetyl-α-L-fucopyranose
≥98%
- Product Code: 103612
CAS:
64913-16-2
Molecular Weight: | 332.31 g./mol | Molecular Formula: | C₁₄H₂₀O₉ |
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EC Number: | MDL Number: | MFCD00069791 | |
Melting Point: | 92-96°C | Boiling Point: | |
Density: | Storage Condition: | -20°C |
Product Description:
1,2,3,4-Tetra-O-acetyl-α-L-fucopyranose is widely used in the synthesis of complex carbohydrates and glycoconjugates. It serves as a key intermediate in the production of fucose-containing oligosaccharides, which are essential for studying biological processes such as cell signaling and immune response. This compound is also employed in the development of glycoproteins and glycolipids, which play crucial roles in cellular recognition and communication. Additionally, it is utilized in the preparation of fucose-based vaccines and therapeutic agents, particularly those targeting bacterial and viral infections. Its acetylated form provides stability and reactivity, making it a valuable building block in carbohydrate chemistry and glycobiology research.
Product Specification:
Test | Specification |
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Appearance | White To Almost White Powder To Crystal |
Purity (%) | 97.5-100 |
Specific Rotation [A]20/D(C=1, CHCl3) | -125--115 |
Infrared Spectrum | Conforms To Structure |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.200 | 10-20 days | ฿2,480.00 |
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1.000 | 10-20 days | ฿5,990.00 |
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1,2,3,4-Tetra-O-acetyl-α-L-fucopyranose
1,2,3,4-Tetra-O-acetyl-α-L-fucopyranose is widely used in the synthesis of complex carbohydrates and glycoconjugates. It serves as a key intermediate in the production of fucose-containing oligosaccharides, which are essential for studying biological processes such as cell signaling and immune response. This compound is also employed in the development of glycoproteins and glycolipids, which play crucial roles in cellular recognition and communication. Additionally, it is utilized in the preparation of fucose-based vaccines and therapeutic agents, particularly those targeting bacterial and viral infections. Its acetylated form provides stability and reactivity, making it a valuable building block in carbohydrate chemistry and glycobiology research.
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