Mannose triflate

98%

Reagent Code: #98212
label
Alias 1,3,4,6-Tetra-O-acetyl-2-O-trifluoromethanesulfonyl-β-D-mannopyranose, TATM, Mannose Triflate
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CAS Number 92051-23-5

science Other reagents with same CAS 92051-23-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 480.36 g/mol
Formula C₁₅H₁₉F₃O₁₂S
badge Registry Numbers
MDL Number MFCD00012353
thermostat Physical Properties
Melting Point 118-122 °C
inventory_2 Storage & Handling
Storage -20°C

description Product Description

Mannose triflate is widely used in organic synthesis as a glycosyl donor for the preparation of complex carbohydrates and glycoconjugates. It is particularly valuable in the synthesis of oligosaccharides due to its high reactivity and selectivity in glycosylation reactions. This compound is employed in the development of glycoproteins, glycolipids, and other biologically active molecules, which are essential for studying cell-cell interactions, immune responses, and pathogen recognition. Additionally, mannose triflate finds applications in the pharmaceutical industry for the production of glycosylated drugs and vaccines, where precise glycosylation is crucial for efficacy and stability. Its role in carbohydrate chemistry also extends to the creation of glycoarrays and probes for biochemical research.

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Test Parameter Specification
Melting Point 0-0
Purity (GC) 98-100%
Chloroform 14-18
Appearance White to off-white powder or crystals
Infrared Spectrum Conforms to Structure
Solubility Colorless clear at 25 mg/mL (2.5%) in CHCl3

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 500mg
10-20 days ฿8,190.00
inventory 100mg
10-20 days ฿2,835.00
inventory 1g
10-20 days ฿11,745.00
inventory 5g
10-20 days ฿44,811.00
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Mannose triflate
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Mannose triflate is widely used in organic synthesis as a glycosyl donor for the preparation of complex carbohydrates and glycoconjugates. It is particularly valuable in the synthesis of oligosaccharides due to its high reactivity and selectivity in glycosylation reactions. This compound is employed in the development of glycoproteins, glycolipids, and other biologically active molecules, which are essential for studying cell-cell interactions, immune responses, and pathogen recognition. Additionally, ma

Mannose triflate is widely used in organic synthesis as a glycosyl donor for the preparation of complex carbohydrates and glycoconjugates. It is particularly valuable in the synthesis of oligosaccharides due to its high reactivity and selectivity in glycosylation reactions. This compound is employed in the development of glycoproteins, glycolipids, and other biologically active molecules, which are essential for studying cell-cell interactions, immune responses, and pathogen recognition. Additionally, mannose triflate finds applications in the pharmaceutical industry for the production of glycosylated drugs and vaccines, where precise glycosylation is crucial for efficacy and stability. Its role in carbohydrate chemistry also extends to the creation of glycoarrays and probes for biochemical research.

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