Ethyl 2-Acetamido-3,4,6-tri-O-acetyl-2-deoxy -1-thio-β-D-galactopyranoside

≥98%

Reagent Code: #103880
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CAS Number 144218-98-4

science Other reagents with same CAS 144218-98-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 391.13 g/mol
Formula C₁₆H₂₅NO₈S
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

This compound is primarily utilized in carbohydrate chemistry and glycobiology research. It serves as a key intermediate in the synthesis of complex oligosaccharides and glycoconjugates. Researchers use it to study glycosylation processes, which are crucial for understanding cell signaling, immune responses, and pathogen interactions. Additionally, it is employed in the development of glycoprotein-based therapeutics and vaccines, where precise control over glycosylation patterns is essential. Its acetylated and thio-modified structure makes it a valuable tool for creating stable and biologically active carbohydrate derivatives.

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Size Availability Unit Price Quantity
inventory 500mg
10-20 days ฿5,445.00
inventory 100mg
10-20 days ฿1,629.00

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Ethyl 2-Acetamido-3,4,6-tri-O-acetyl-2-deoxy -1-thio-β-D-galactopyranoside
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This compound is primarily utilized in carbohydrate chemistry and glycobiology research. It serves as a key intermediate in the synthesis of complex oligosaccharides and glycoconjugates. Researchers use it to study glycosylation processes, which are crucial for understanding cell signaling, immune responses, and pathogen interactions. Additionally, it is employed in the development of glycoprotein-based therapeutics and vaccines, where precise control over glycosylation patterns is essential. Its acetyla

This compound is primarily utilized in carbohydrate chemistry and glycobiology research. It serves as a key intermediate in the synthesis of complex oligosaccharides and glycoconjugates. Researchers use it to study glycosylation processes, which are crucial for understanding cell signaling, immune responses, and pathogen interactions. Additionally, it is employed in the development of glycoprotein-based therapeutics and vaccines, where precise control over glycosylation patterns is essential. Its acetylated and thio-modified structure makes it a valuable tool for creating stable and biologically active carbohydrate derivatives.

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