N-[(1R,2R)-2-(diMethylaMino)-1,2-diphenylethyl]-N'-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)- Thiourea
98%
- Product Code: 70669
CAS:
1440198-44-6
| Molecular Weight: | 629.72 g./mol | Molecular Formula: | C₃₁H₃₉N₃O₉S |
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| EC Number: | MDL Number: | ||
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| Density: | Storage Condition: | 2-8°C |
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.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.025 | 10-20 days | €157.66 |
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| 0.100 | 10-20 days | €470.60 |
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N-[(1R,2R)-2-(diMethylaMino)-1,2-diphenylethyl]-N'-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)- Thiourea
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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