2,3,4,6-Tetra-O-benzyl-α-D-glucopyranosyl p-Trifluoromethylbenzylthio-N-(p-trifluoromethylphenyl)formimidate

≥95%

Reagent Code: #103659
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CAS Number 468095-63-8

science Other reagents with same CAS 468095-63-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 901.96 g/mol
Formula C₅₀H₄₅F₆NO₆S
badge Registry Numbers
MDL Number MFCD06797177
thermostat Physical Properties
Melting Point 120-125°C
inventory_2 Storage & Handling
Storage -20°C

description Product Description

This compound is primarily utilized in organic synthesis, particularly in the preparation of complex carbohydrate derivatives. It serves as a key glycosyl donor in glycosylation reactions, enabling the formation of glycosidic bonds with high selectivity and efficiency. Its application is significant in the development of glycoconjugates, which are essential in the study of biological processes and the design of carbohydrate-based drugs. Additionally, it is crucial for constructing oligosaccharides and polysaccharides with specific structural features. Its use extends to research in glycobiology, where it aids in understanding the role of carbohydrates in cellular interactions and signaling pathways. The compound’s stability and reactivity make it a valuable tool in the synthesis of biologically active molecules and potential therapeutic agents.

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Size Availability Unit Price Quantity
inventory 200mg
10-20 days ฿5,454.00

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2,3,4,6-Tetra-O-benzyl-α-D-glucopyranosyl p-Trifluoromethylbenzylthio-N-(p-trifluoromethylphenyl)formimidate
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This compound is primarily utilized in organic synthesis, particularly in the preparation of complex carbohydrate derivatives. It serves as a key glycosyl donor in glycosylation reactions, enabling the formation of glycosidic bonds with high selectivity and efficiency. Its application is significant in the development of glycoconjugates, which are essential in the study of biological processes and the design of carbohydrate-based drugs. Additionally, it is crucial for constructing oligosaccharides and po

This compound is primarily utilized in organic synthesis, particularly in the preparation of complex carbohydrate derivatives. It serves as a key glycosyl donor in glycosylation reactions, enabling the formation of glycosidic bonds with high selectivity and efficiency. Its application is significant in the development of glycoconjugates, which are essential in the study of biological processes and the design of carbohydrate-based drugs. Additionally, it is crucial for constructing oligosaccharides and polysaccharides with specific structural features. Its use extends to research in glycobiology, where it aids in understanding the role of carbohydrates in cellular interactions and signaling pathways. The compound’s stability and reactivity make it a valuable tool in the synthesis of biologically active molecules and potential therapeutic agents.

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