N-[(1S,2S)-2-(diMethylaMino)-1,2-diphenylethyl]-N'-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)- Thiourea
98%
- Product Code: 70716
CAS:
1414889-04-5
| Molecular Weight: | 629.72106 g./mol | Molecular Formula: | C₃₁H₃₉N₃O₉S |
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| Density: | Storage Condition: | 2-8°C |
Product Description:
This compound is primarily utilized in the field of organic synthesis, particularly in the development of glycosylation reactions. It serves as a key intermediate in the preparation of complex carbohydrate structures, which are essential in the study of glycobiology and the development of glycoconjugate vaccines. Its thiourea moiety enhances its ability to act as a catalyst or a chiral auxiliary in asymmetric synthesis, making it valuable for the production of enantiomerically pure compounds. Additionally, it finds application in medicinal chemistry for the design and synthesis of glycosidase inhibitors, which are potential therapeutic agents for diseases like diabetes and viral infections. Its acetyl-protected sugar moiety allows for selective deprotection, enabling precise modifications in carbohydrate-based drug development.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.010 | 10-20 days | ฿4,500.00 |
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| 0.050 | 10-20 days | ฿17,838.00 |
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N-[(1S,2S)-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 organic synthesis, particularly in the development of glycosylation reactions. It serves as a key intermediate in the preparation of complex carbohydrate structures, which are essential in the study of glycobiology and the development of glycoconjugate vaccines. Its thiourea moiety enhances its ability to act as a catalyst or a chiral auxiliary in asymmetric synthesis, making it valuable for the production of enantiomerically pure compounds. Additionally, it finds application in medicinal chemistry for the design and synthesis of glycosidase inhibitors, which are potential therapeutic agents for diseases like diabetes and viral infections. Its acetyl-protected sugar moiety allows for selective deprotection, enabling precise modifications in carbohydrate-based drug development.
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