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

≥98%

Reagent Code: #103995
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CAS Number 187022-49-7

science Other reagents with same CAS 187022-49-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 572.83 g/mol
Formula C₂₁H₂₄Cl₃NO₉S
badge Registry Numbers
MDL Number MFCD11112181
thermostat Physical Properties
Melting Point 143°C(lit.)
inventory_2 Storage & Handling
Storage -20°C

description Product Description

This compound is primarily utilized in the field of organic synthesis, particularly in the preparation of complex carbohydrates and glycoconjugates. It serves as a key intermediate in the synthesis of glycosyl donors, which are essential for constructing glycosidic bonds in oligosaccharides. The presence of protective groups, such as acetyl and trichloroethoxyformamido, allows for selective deprotection and further functionalization, making it a versatile building block in carbohydrate chemistry. Additionally, its thio-glycoside moiety enhances its stability and reactivity, facilitating its use in glycosylation reactions. This compound is particularly valuable in the development of biologically active molecules, including glycopeptides and glycolipids, which have applications in drug discovery and biochemical research.

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inventory 1g
10-20 days ฿3,780.00

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Phenyl 3,4,6-Tri-O-acetyl-2-deoxy-1-thio-2-(2,2,2-trichloroethoxyformamido)-β-D-glucopyranoside
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This compound is primarily utilized in the field of organic synthesis, particularly in the preparation of complex carbohydrates and glycoconjugates. It serves as a key intermediate in the synthesis of glycosyl donors, which are essential for constructing glycosidic bonds in oligosaccharides. The presence of protective groups, such as acetyl and trichloroethoxyformamido, allows for selective deprotection and further functionalization, making it a versatile building block in carbohydrate chemistry. Additionally, its thio-glycoside moiety enhances its stability and reactivity, facilitating its use in glycosylation reactions. This compound is particularly valuable in the development of biologically active molecules, including glycopeptides and glycolipids, which have applications in drug discovery and biochemical research.
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