2-[2-(2-Azidoethoxy)ethoxy]ethyl 2,3,4,6-Tetra-O-acetyl-D-galactopyranoside

95%

  • Product Code: 95825
  CAS:    381716-33-2
Molecular Weight: 505.48 g./mol Molecular Formula: C₂₀H₃₁N₃O₁₂
EC Number: MDL Number: MFCD00191441
Melting Point: Boiling Point:
Density: Storage Condition: room temperature
Product Description: This chemical is primarily used in the synthesis of complex carbohydrates and glycoconjugates. It serves as a key intermediate in the preparation of glycosylated molecules, which are essential in studying biological processes such as cell signaling and immune responses. The azide group allows for efficient conjugation via click chemistry, enabling the attachment of various functional groups or labels for research purposes. Additionally, its acetyl-protected galactose moiety is valuable in the development of glycoproteins and glycolipids, which have applications in vaccine development and drug delivery systems. Its role in glycobiology research makes it a crucial tool for understanding and manipulating carbohydrate-based interactions in biological systems.
Product Specification:
Test Specification
APPEARANCE PALE YELLOW TO REDDISH YELLOW LIQUID
PURITY 94.5-100
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.100 10-20 days ฿4,380.00
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-
0.500 10-20 days ฿19,960.00
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-
2-[2-(2-Azidoethoxy)ethoxy]ethyl 2,3,4,6-Tetra-O-acetyl-D-galactopyranoside
This chemical is primarily used in the synthesis of complex carbohydrates and glycoconjugates. It serves as a key intermediate in the preparation of glycosylated molecules, which are essential in studying biological processes such as cell signaling and immune responses. The azide group allows for efficient conjugation via click chemistry, enabling the attachment of various functional groups or labels for research purposes. Additionally, its acetyl-protected galactose moiety is valuable in the development of glycoproteins and glycolipids, which have applications in vaccine development and drug delivery systems. Its role in glycobiology research makes it a crucial tool for understanding and manipulating carbohydrate-based interactions in biological systems.
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