169532-17-6

Basic information

• Product Name: Ethyl 2,3,4-Tri-O-benzyl-1-thio-α,-L-fucopyranoside
• Synonyms: Ethyl 2,3,4-Tri-O-benzyl-1-thio-α,-L-fucopyranoside;Ethyl 6-Deoxy-2,3,4-tris-O-(phenylMethyl)-1-thio-L-galactopyranoside;L-Galactopyranoside, ethyl 6-deoxy-2,3,4-tris-O-(phenylMethyl)-1-thio-
• CAS NO: 169532-17-6
• Molecular Formula: C₂₉H₃₄O₄S
• Molecular Weight: 478.64286
• Product Categories: Carbohydrates & Derivatives
• Mol File: 169532-17-6.mol
• Article Data: 1

Chemical Properties

• Appearance: /
• Storage Temp.: -20°C Freezer, Under inert atmosphere
• Solubility: Chloroform (Slightly), Methanol (Slightly)
• CAS DataBase Reference: Ethyl 2,3,4-Tri-O-benzyl-1-thio-α,-L-fucopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: Ethyl 2,3,4-Tri-O-benzyl-1-thio-α,-L-fucopyranoside(169532-17-6)
• EPA Substance Registry System: Ethyl 2,3,4-Tri-O-benzyl-1-thio-α,-L-fucopyranoside(169532-17-6)

Safety Data

• Hazardous Substances Data: 169532-17-6(Hazardous Substances Data)

Usage

Description

Ethyl 2,3,4-Tri-O-benzyl-1-thio-α,-L-fucopyranoside is a complex organic compound that serves as a key intermediate in the synthesis of various biologically significant molecules, particularly those involving L-fucose, a sugar commonly found in many biological systems.

Uses

Used in Pharmaceutical Industry:
Ethyl 2,3,4-Tri-O-benzyl-1-thio-α,-L-fucopyranoside is used as a synthetic building block for the creation of complex oligosaccharides containing L-fucose. These oligosaccharides are essential components of many biological molecules, such as glycoproteins and glycolipids, which play crucial roles in cellular recognition, signaling, and immune response. The compound's utility in this application is due to its ability to facilitate the synthesis of these complex structures, which can be challenging to produce directly from simpler precursors.
Used in Chemical Research:
In the field of chemical research, Ethyl 2,3,4-Tri-O-benzyl-1-thio-α,-L-fucopyranoside is used as a valuable reagent for studying the chemical properties and reactivity of L-fucose-containing compounds. This is particularly important for understanding the role of these molecules in various biological processes and for developing new strategies to target them for therapeutic purposes.
Used in Material Science:
Ethyl 2,3,4-Tri-O-benzyl-1-thio-α,-L-fucopyranoside may also find applications in material science, particularly in the development of novel materials with specific properties. The compound's unique structure and reactivity can be exploited to create new materials with tailored characteristics, such as improved biocompatibility or enhanced interaction with biological systems.

Downstream Products

• 906650-21-3 Acetic acid (2R,3S,4R,5R,6S)-5-benzenesulfonylamino-4-benzyloxy-2-benzyloxymethyl-6-[(2R,3S,4R)-4-benzyloxy-2-((2R,3S,4R,5R,6S)-3,4,5-tris-benzyloxy-6-methyl-tetrahydro-pyran-2-yloxymethyl)-3,4-dihydro-2H-pyran-3-yloxy]-tetrahydro-pyran-3-yl ester 
• 1026074-30-5 (1R,2R,4R,6S)-2-tert-butyldimethylsilyloxy-4-hydroxymethyl-6-methylcyclohexyl 2,3,4-tri-O-benzyl-6-deoxy-α-L-galactopyranoside 
• 1026074-32-7 (1R,2R,4R,6S)-2-tert-butyldimethylsilyloxy-4-chloromethyl-6-methylcyclohexyl 2,3,4-tri-O-benzyl-6-deoxy-α-L-galactopyranoside 
• 1026074-33-8 (1R,2R,4R,6S)-2-tert-butyldimethylsilyloxy-4,6-dimethylcyclohexyl 2,3,4-tri-O-benzyl-6-deoxy-α-L-galactopyranoside 
• 1026073-51-7 methyl (1R,3R,4R,5S)-4-O-(2,3,4-tris-O-benzyl-6-deoxy-α-L-galactopyranosyl)-3,4-dihydroxy-5-methylcyclohexane-1-carboxylate 
• 1334630-94-2 3-(benzyloxycarbonylamino)propyl O-(2,3,4-tri-O-benzyl-α-L-fucopyranosyl)-(1→2)-O-(6-O-benzyl-3,4-O-isopropylidene-β-D-galactopyranosyl)-(1→4)-6-O-t-butyldiphenylsilyl-2-deoxy-2-phthalimido-β-D-glucopyranoside 
• 1334631-07-0 3-(benzyloxycarbonylamino)propyl O-(2,3,4-tri-O-acetyl-6-O-benzyl-β-D-galactopyranosyl)-(1→4)-[O-(2,3,4-tri-O-benzyl-α-L-fucopyranosyl)-(1→3)]-6-O-t-butyldiphenylsilyl-2-deoxy-2-phthalimido-β-D-glucopyranoside 
• 178454-13-2 (2R,3R)-2-hydroxy-3-(3,4,5-tri-O-benzyl-α-L-fucopyranos-l-yl)-succinic acid dimethyl ester 

Relevant articles and documents

SPECIFIC ANTAGONIST FOR BOTH E- AND P-SELECTINS

Compounds and methods are provided for modulating in vitro and in vivo processes mediated by selectin binding. More specifically, selectin modulators and their use are described, wherein the selectin modulators that modulate (e.g., inhibit or enhance) a selectin-mediated function comprise a particular glycomimetic linked to a particular BASA (Benzyl Amino Sulfonic Acid).