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
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
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
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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