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

98%

Reagent Code: #70669
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CAS Number 1440198-44-6

science Other reagents with same CAS 1440198-44-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 629.72 g/mol
Formula C₃₁H₃₉N₃O₉S
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This compound is primarily utilized in the field of medicinal chemistry and drug development, particularly in the synthesis of glycosylated compounds. It serves as a key intermediate in the preparation of glycosylthiourea derivatives, which are explored for their potential biological activities, including antimicrobial and anticancer properties. The presence of the acetyl-protected glucopyranosyl moiety allows for selective deprotection and further functionalization, making it valuable in the design of carbohydrate-based therapeutics. Additionally, it is employed in studies focusing on carbohydrate-protein interactions, aiding in the development of glycoconjugate vaccines and enzyme inhibitors. Its stereochemistry also makes it useful in asymmetric synthesis, contributing to the production of chiral molecules with high enantiomeric purity.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿5,976.00
inventory 100mg
10-20 days ฿17,838.00

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N-[(1R,2R)-2-(diMethylaMino)-1,2-diphenylethyl]-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 medicinal chemistry and drug development, particularly in the synthesis of glycosylated compounds. It serves as a key intermediate in the preparation of glycosylthiourea derivatives, which are explored for their potential biological activities, including antimicrobial and anticancer properties. The presence of the acetyl-protected glucopyranosyl moiety allows for selective deprotection and further functionalization, making it valuable in the design of c

This compound is primarily utilized in the field of medicinal chemistry and drug development, particularly in the synthesis of glycosylated compounds. It serves as a key intermediate in the preparation of glycosylthiourea derivatives, which are explored for their potential biological activities, including antimicrobial and anticancer properties. The presence of the acetyl-protected glucopyranosyl moiety allows for selective deprotection and further functionalization, making it valuable in the design of carbohydrate-based therapeutics. Additionally, it is employed in studies focusing on carbohydrate-protein interactions, aiding in the development of glycoconjugate vaccines and enzyme inhibitors. Its stereochemistry also makes it useful in asymmetric synthesis, contributing to the production of chiral molecules with high enantiomeric purity.

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