N-[(1R,2R)-2-Aminocyclohexyl]-N'-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)thiourea

≥98%,99%d.e.

Reagent Code: #70695
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CAS Number 933456-75-8

science Other reagents with same CAS 933456-75-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 503.6 g/mol
Formula C₂₁H₃₃N₃O₉S
thermostat Physical Properties
Melting Point 150°C(decomp)
inventory_2 Storage & Handling
Storage room temperature, dry

description Product Description

This compound is primarily utilized in the field of carbohydrate chemistry and glycobiology research. It serves as a key intermediate in the synthesis of glycosyl thiourea derivatives, which are valuable for studying carbohydrate-protein interactions. These interactions are crucial for understanding biological processes such as cell signaling, immune response, and pathogen recognition. Additionally, the compound is used in the development of glycosidase inhibitors, which have potential therapeutic applications in treating diseases like diabetes, viral infections, and certain cancers. Its acetylated sugar moiety makes it suitable for selective deprotection strategies, enabling the creation of diverse glycosylated compounds for further biological evaluation.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿14,900.00

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N-[(1R,2R)-2-Aminocyclohexyl]-N'-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)thiourea
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This compound is primarily utilized in the field of carbohydrate chemistry and glycobiology research. It serves as a key intermediate in the synthesis of glycosyl thiourea derivatives, which are valuable for studying carbohydrate-protein interactions. These interactions are crucial for understanding biological processes such as cell signaling, immune response, and pathogen recognition. Additionally, the compound is used in the development of glycosidase inhibitors, which have potential therapeutic applic

This compound is primarily utilized in the field of carbohydrate chemistry and glycobiology research. It serves as a key intermediate in the synthesis of glycosyl thiourea derivatives, which are valuable for studying carbohydrate-protein interactions. These interactions are crucial for understanding biological processes such as cell signaling, immune response, and pathogen recognition. Additionally, the compound is used in the development of glycosidase inhibitors, which have potential therapeutic applications in treating diseases like diabetes, viral infections, and certain cancers. Its acetylated sugar moiety makes it suitable for selective deprotection strategies, enabling the creation of diverse glycosylated compounds for further biological evaluation.

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