Phenyl 3,4,6-Tri-O-acetyl-2-deoxy-1-thio-2-(2,2,2-trichloroethoxyformamido)-β-D-glucopyranoside
≥98%
Reagent
Code: #103995
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.
shopping_cart Available Sizes & Pricing
Cart
No products
Subtotal:
0.00
Total
0.00
THB