Phenyl 3,4,6-Tri-O-acetyl-2-deoxy-1-thio-2-(2,2,2-trichloroethoxyformamido)-β-D-galactopyranoside

≥98%

Reagent Code: #103994
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CAS Number 278784-83-1

science Other reagents with same CAS 278784-83-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 572.83 g/mol
Formula C₂₁H₂₄Cl₃NO₉S
thermostat Physical Properties
Melting Point 115-119°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This compound is primarily utilized in the synthesis of complex carbohydrates and glycoconjugates, playing a critical role in carbohydrate chemistry research. It serves as a key intermediate in the preparation of oligosaccharides, which are essential for studying biological processes such as cell signaling and immune responses. The acetyl and trichloroethoxyformamido groups provide protection for specific reactive sites, enabling selective glycosylation reactions. This selectivity is crucial for constructing well-defined carbohydrate structures, which are often used in the development of vaccines, diagnostic tools, and therapeutic agents targeting glycoprotein-related diseases. Additionally, its thio-glycoside moiety enhances its stability and reactivity, making it a valuable building block in synthetic organic chemistry.

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Test Parameter Specification
Appearance White to Almost White Powder to Crystal
Purity (%) 98-100
Melting Point (\u2103) 115.0-119.0
Specific Rotation [A]20/D (C=1, CHCl3)(\u00b0) -6--4
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿2,277.00

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Phenyl 3,4,6-Tri-O-acetyl-2-deoxy-1-thio-2-(2,2,2-trichloroethoxyformamido)-β-D-galactopyranoside
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This compound is primarily utilized in the synthesis of complex carbohydrates and glycoconjugates, playing a critical role in carbohydrate chemistry research. It serves as a key intermediate in the preparation of oligosaccharides, which are essential for studying biological processes such as cell signaling and immune responses. The acetyl and trichloroethoxyformamido groups provide protection for specific reactive sites, enabling selective glycosylation reactions. This selectivity is crucial for construc

This compound is primarily utilized in the synthesis of complex carbohydrates and glycoconjugates, playing a critical role in carbohydrate chemistry research. It serves as a key intermediate in the preparation of oligosaccharides, which are essential for studying biological processes such as cell signaling and immune responses. The acetyl and trichloroethoxyformamido groups provide protection for specific reactive sites, enabling selective glycosylation reactions. This selectivity is crucial for constructing well-defined carbohydrate structures, which are often used in the development of vaccines, diagnostic tools, and therapeutic agents targeting glycoprotein-related diseases. Additionally, its thio-glycoside moiety enhances its stability and reactivity, making it a valuable building block in synthetic organic chemistry.

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